Cyclic amine compounds and pharmaceutical composition containing the same

ABSTRACT

A cyclic amine compound by the following general formula (1):                    
     wherein, 
     R 1 , R 2  and R 3  each independently represent a hydrogen atom or an alkoxy group 
     W 1  and W 2  each independently represent N or CH; 
     X represents O, NR 4 , CONR 4  or NR 4 CO; 
     R 4  represents a hydrogen atom, or an alkyl, aryl, heteroaryl, aralkyl, or heteroaralkyl group; and 
     l, m and n each represents a number of 0 or 1, a salt thereof and a hydrate thereof are provided. These compounds have inhibitory effects on both cell adhesion and cell infiltration and are useful as anti-asthmatic agents, anti-allergic agents, anti-rheumatic agents, anti-arteriosclerotic agents, anti-inflammatory agents, anti-Sjogren&#39;s syndrome agents or the like.

This application is a continuation-in-part of U.S patent application Ser. No. 09/983,928, filed on Oct. 26, 2001, now U.S. Pat No. 6,498,169, and a Continuation-in-part of U.S. patent application Ser. No. 09/941,684, filed on Aug. 30, 2001, now U.S. Pat. No. 6,395,753.

INCORPORATED BY REFERENCE

Each document, patent application or patent publication cited by or referred to in this disclosure is incorporated by reference in its entirety. Any patent document to which this application claims priority is also incorporated by reference in its entirety. Specifically, priority documents Ser. No. 09/941,684, filed Aug. 30, 2001 and Ser. No. 09/983,928, filed Oct. 26, 2001 are hereby incorporated by reference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to novel cyclic amine compounds which have inhibitory effects on both cell adhesion and cell infiltration and are useful as anti-asthmatic agents, anti-allergic agents, anti-rheumatic agents, anti-arteriosclerotic agents, anti-inflammatory agents, anti-Sjogren's syndrome agents or the like, and medicines containing such compounds.

2. Description of the Background Art

In various inflammatory diseases, infiltration of leukocytes into inflammatory sites is observed. For example, infiltration of eosinophils into the bronchus in asthma (Ohkawara, Y. et al., Am. J. Respir. Cell Mol. Biol., 12, 4-12 (1995)), infiltration of macrophages and T lymphocytes into the aorta in arteriosclerosis (Sakai, A. et al., Arterioscler Thromb. Vasc. Biol., 17, 310-316 (1997)), infiltration of T lymphocytes and eosinophils into the skin in atopic dermatitis (Wakita, H. et al., J. Cutan. Pathol., 21, 33-39 (1994)) or contact dermatitis (Satoh, T. et al., Eur. J. Immunol., 27 85-91 (1997)), and infiltration of various leukocytes into rheumatoid synovial tissue (Tak, P P. et al., Clin. Immunol. Immunopathol., 77, 236-242 (1995)), have been reported. Sjogren's syndrome in humans is an organ-specific autoimmune disease characterized by lymphocytic infiltration into the salivary and lacrimal glands, resulting in symptoms of dry mouth and dry eye due to insufficient secretion (Fox R I et al.: “Sjogren's syndrome: proposed criteria for classification” Arthritis Rheum 1986, 29: 577-585).

Infiltration of these leukocytes is elicited by cytokines, chemokines, lipids, and complements produced in inflammatory sites (Albelda, S M. et al., FASEB J., 8, 504-512 (1994)). Activated leukocytes adhere to vascular endothelial cells through an interaction called rolling or tethering with endothelial cells activated likewise. Thereafter, the leukocytes transmigrate through endothelium to infiltrate into the inflammatory sites (Springer, T A., Annu. Rev. Physiol., 57, 827-872 (1995)). In adhesion of leukocytes to the vascular endothelial cells in this process, various cell adhesion molecules such as an immunoglobulin superfamily (ICAM-1, VCAM-1 and the like), a selectin family (E-selectin and the like), an integrin family (LFA-1, VLA-4 and the like) and CD44, which are induced on the surfaces of the cells by stimulation by cytokines or the like, play important roles (“Rinsho Meneki (Clinical Immune)”, 30, Supple. 18 (1998)), and a relationship between the disorder state and aberrant expression of the cell adhesion molecules is noted.

Accordingly, an agent capable of inhibiting cell adhesion or cell infiltration can be useful as an agent for preventing and treating allergic diseases such as bronchial asthma, dermatitis, rhinitis and conjunctivitis; autoimmune diseases such as rheumatoid arthritis, nephritis, Sjogren's syndrome, inflammatory bowel diseases, diabetes and arteriosclerosis; and chronic inflammatory diseases. In fact, it has been reported that antibodies against adhesion molecules or leukocytes such as LFA-1, Mac-1 and VLA-4 on antibodies against ICAM-1, VCAM-1, P-selectin, E-selectin and the like on vascular endothelial cells, which become ligands thereof, inhibit infiltration of leukocytes into inflammatory sites in animal models. For example, neutralizing antibodies against VCAM-1 and VLA-4, which is a counter receptor thereof, can delay development of diabetes in an NOD mouse model which spontaneously causes the diabetes (Michie, S A. et al., Curr. Top. Microbiol. Immunol., 231 65-83 (1998)). It has also been reported that an antibody against VLA-4 or ICAM-1 and its counter receptor, LFA-1, inhibits infiltration of eosinophils in a guinea pig and mouse allergic conjunctivitis model (Ebihara et al., Current Eye Res., 19, 20-25 (1999); Whitcup, S M et al., Clin. Immunol., 93, 107-113 (1999)), and a monoclonal antibody against VCAM-1 inhibits infiltration of leukocytes in a mouse DSS-induced colitis model to attenuate colitis (Soriano, A. et al., Lab. Invest., 80, 1541-1551 (2000)). Further, an anti-VLA-4 antibody and an anti-CD44 antibody reduce the incidence of disease symptoms in a mouse collagen arthritis model (Zeidler, A. et al., Autoimmunity, 21, 245-252 (1995)). Even in cell adhesion molecule deficient-mice, inhibition of infiltration of leukocytes into inflammatory tissues is observed likewise in inflammatory models (Bendjelloul, F. et al., Clin. Exp. Immunol., 119, 57-63 (2000); Wolyniec, W W. et al., Am. J. Respir. Cell Mol. Biol., 18, 777-785 (1998); Bullard, D C. et al., J. Immunol., 157, 3153-3158 (1996)).

However, it is difficult to develop antibody-based drugs because they are polypeptides and so oral administration is a problem. Moreover, the possible side effects due to antigenicity and allergic reactions are problems.

On the other hand, there have been various investigations of low-molecular weight compounds having an inhibitory effect on cell adhesion with a view toward permitting oral administration. These compounds include benzothiophene derivatives (Boschelli, D H. et al., J. Med. Chem., 38, 4597-4614 (1995)), naphthalene derivatives (Japanese Patent Application Laid-Open No. 10-147568), hydroxybenzoic acid derivatives (Japanese Patent Application Laid-Open No. 10-182550), lignans (Japanese Patent Application Laid-Open No. 10-67656), 2-substituted benzothiazole derivatives (Japanese Patent Application Laid-Open No. 2000-086641 through PCT route), condensed pyrazine compounds (Japanese Patent Application Laid-Open No. 2000-319277 through PCT route), 2,6-dialkyl-4-silylphenol (Japanese Patent Application Laid-Open No. 2000-509070 through PCT route) and the like. However, the goal has not often been sufficiently achieved under the circumstances. Cyclic diamine compounds described in Japanese Patent Application Laid-Open Nos. 9-143075 and 11-92382 and Japanese Patent Application No. 2000-271220 do not exhibit a sufficient inhibitory effect on cell adhesion, and so there is a demand for further improvement in activity.

SUMMARY OF THE INVENTION

An object of the present invention is to provide a substance having inhibitory effects on both cell adhesion and cell infiltration, plus excellent anti-asthmatic effects, anti-allergic effects, anti-rheumatic effects, anti-arteriosclerotic effects, anti-inflammatory effects and anti-Sjogren's syndrome effect.

With the foregoing circumstances in mind, the present inventors carried out an extensive investigation to find a substance which inhibits cell adhesion and cell infiltration. As a result, we found that compounds represented by the general formula (1) having phenyl-pyridyl or biphenyl groups at both ends of the cyclic amine, have excellent cell adhesion-inhibiting effects and cell infiltration-inhibiting effects and are useful as anti-allergic agents, anti-asthmatic agents, anti-rheumatic agents, anti-arteriosclerotic agents or anti-inflammatory agents or anti-Sjogren's syndrome agents.

The present invention provides a cyclic amine compound represented by the following general formula (1):

wherein,

R¹, R² and R³ each independently represent a hydrogen atom, a halogen atom, or hydroxy, alkyl, halogen-substituted alkyl, alkoxy, alkylthio, carboxyl, alkoxycarbonyl or alkanoyl group;

W¹ and W² each independently represent N or CH;

X represents O, NR⁴, CONR⁴ or NR⁴CO;

l, m and n each represents a number of 0 or 1.

R⁴ represents a hydrogen atom, or an alkyl, alkenyl, alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted aralkyl, or substituted or unsubstituted heteroalkyl group; and

According to the present invention, there is also provided a medicine comprising the above cyclic amine compound, a salt thereof, or a hydrate thereof as an active ingredient.

According to the present invention, there is further provided a pharmaceutical composition comprising the above cyclic amine compound, the salt thereof, or the hydrate thereof and a pharmaceutically acceptable carrier.

According to the present invention, there is still further provided a method for treating a disease caused by cell adhesion and/or cell infiltration, which comprises administering an effective amount of the above cyclic amine compound, a salt thereof, or a hydrate thereof to a patient who requires such treatment.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The compound of the present invention is characterized in that the cyclic amine has two phenyl-pyridyl or biphenyl groups, or phenyl-pyridyl and biphenyl groups. It has not been known at all that compounds having such structure have both of excellent cell adhesion-inhibiting effects and cell infiltration-inhibiting effects.

In the general formula (1), the halogen atoms for R¹, R² and R³ include fluorine, chlorine, bromine and iodine atoms.

The alkyl group for R¹, R², R³ and R⁴ typically includes straight, branched or cyclic C₁-C₈ alkyl groups, such as straight or branched C₁-C₈ alkyl groups, for example, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl and octyl groups, and C₃-C₈ cycloalkyl groups, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclohexylmethyl and cyclohexylethyl groups. Among them, particularly preferred are C₁-C₆ alkyl groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl and the like.

The halogen-substituted alkyl group for R¹, R² and R³ typically includes C₁-C₈ alkyl groups substituted with 1 to 3 halogen atoms. Among them, particularly preferred are C₁-C₆ alkyl groups substituted with 1 to 3 halogen atoms, such as trifluoromethyl, 2,2,2-trifluoroethyl, etc.

The alkoxy group typically includes straight, branched or cyclic C₁-C₈ alkoxy groups, such as straight or branched C₁-C₈ alkoxy groups, for example, methoxy, ethoxy, propoxy, butoxy, pentyloxy and hexyloxy groups; and C₃-C₈ cycloalkyloxy groups, for example, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, cyclohexylmethyloxy and cyclohexylethyloxy groups. Among them, particularly preferred are C₁-C₆ alkoxy groups such as methoxy, ethoxy, n-popoxy, isopropoxy and n-butyloxy groups.

The alkylthio group typically includes C₁-C₈ alkylthio groups, and is preferably a C₁-C₆ alkylthio group such as, for example, methylthio, ethylthio, n-propylthio, isopropylthio or the like.

The alkoxycarbonyl group typically includes C₁-C₆ alkoxycarbonyl groups, and is preferably a C₁-C₆ alkoxycarbonyl group such as methoxycarbonyl, ethoxycarbonyl, tert-butoxycarbonyl or the like.

The alkanoyl group typically includes C₁-C₆ alkanoyl groups and is preferably a C₁-C₄ alkanoyl group such as acetyl, propionyl, butyryl, isobutyryl or the like.

The alkenyl group for R⁴ typically includes C₃-C₈ alkenyl groups and is preferably a C₃-C₆ alkenyl group such as 2-propenyl, 3-butenyl or the like. The alkynyl group typically includes C₃-C₈ alkynyl groups and is preferably a C₃-C₆ alkynyl group such as 2-propynyl, 3-butynyl or the like.

The aryl group for R⁴ typically includes C₆-C₁₄ aryl groups and is preferably phenyl, naphthyl, anthryl, indenyl, indanyl, 5,6,7,8-tetrahydronaphthyl or the like. The heteroaryl group for R⁴ typically includes heteroaryl groups of 5- or 6-membered ring containing 1 to 4 nitrogen atoms in the ring, and is preferably imidazolyl, pyridyl, pyrimidinyl or the like. The aralkyl group typically includes C₆-C₁₄ aryl-C₁-C₆ alkyl groups such as phenyl C₁-C₆ alkyl groups and naphthyl C₁-C₆ alkyl groups, for example, benzyl, naphthylmethyl, phenylethyl, phenylpropyl, etc. The heteroaralkyl group typically includes 5- or 6-membered ring heteroaryl containing 1 to 4 nitrogen atoms-C₁-C₆ alkyl groups, such as imidazolyl-C₁-C₆ alkyl, pyridyl-C₁-C₆ alkyl, pyrimidinyl-C₁-C₆ alkyl, etc.

The groups which can substitute the above-mentioned aryl, heteroaryl, aralkyl and heteroaralkyl include 1 to 3 groups or atoms selected from alkyl, alkoxy, halogen-substituted alkoxy, alkylthio, halogen, nitro, amino, acetylamino, trifluoromethyl and alkylenedioxy, wherein said alkyl, alkoxy and alkylthio include those illustrated for R¹˜R³. The halogen-substituted alkoxy includes C₁-C₈ alkoxy groups substituted by 1 to 3 halogen atoms, and is preferably a C₁-C₆ alkoxy group substituted by 1 to 3 halogen atoms such as trifluoromethoxy or 2,2,2-trifluoroethoxy. The alkylenedioxy group typically includes C₁-C₃ alkylenedioxy groups such as methylenedioxy, ethylenedioxy and propylenedioxy groups.

Preferably, X represents NR⁴. More preferably, X represents NR⁴ and R⁴ represents a substituted or unsubstituted C₆-C₁₄ aryl group or a substituted or unsubstituted 5- or 6-membered ring heteroaryl group containing 1 to 4 nitrogen atoms in the ring. The compounds of the formula (1) wherein X represents NR⁴ have particularly strong cell adhesion-inhibiting action as shown later in Test Example 1.

Preferably, R¹, R² and R³ are attached to the phenyl group at the 3, 4 and 5-positions thereof. In this case, it is more preferable that R¹ and R³ (at the 3- and 5-positions of the phenyl ring) are an alkoxy group or a halogen. It is also preferable that R² (at the 4-position of the phenyl ring) is a hydrogen atom, a halogen atom, or a hydroxy, alkyl, halogen-substituted alkyl, alkoxy, alkylthio, carboxy, alkoxycarbonyl or alkanoyl group. I denotes 0 or 1, and is preferably 1.

Preferably, W¹ represents N.

Preferably, W² represents N.

Most preferable compounds include the compounds of the formula (1), wherein X represents NR⁴, and R⁴ represents a substituted or unsubstituted C₆-C₁₄ aryl group or a substituted or unsubstituted 5- or 6-membered ring heteroaryl group containing 1 to 4 nitrogen atoms in the ring. Particularly preferably, R⁴ represents a phenyl or pyridyl group which may be substituted with one or two groups or atoms selected from halogen, alkyl, alkoxy, alkylthio, trifluoromethyl and alkylenedioxy.

No particular limitation is imposed on the salts of the compounds (1) according to the invention as long as they are pharmaceutically acceptable salts. Examples include the acid-addition salts of mineral acids, such as hydrochlorides, hydrobromides, hydroiodides, sulfates and phosphates; and acid-addition salts of organic acids, such as benzoates, methanesulfonates, ethanesulfonates, benzenesulfonates, p-toluenesulfonates, oxalates, maleates, fumarates, tartrates, citrates and acetates.

The compounds of formula (1) may be present in the form of solvates typified by hydrates, and the solvates are embraced in the present invention.

The compounds of formula (1) can be prepared in accordance with the following processes A˜K:

Process A: Preparation of the compound of the formula (1) wherein l=1, m=0, n=1 and X=CONR⁴

wherein, W¹, W², R¹, R², R³ and R⁴ are as defined above, W³ has the same meaning as W¹ or W², and B denotes a leaving group such as a halogen atom, or methanesulfonyloxy or p-toluenesulfonyloxy group.

Compound (2) and an N-(2-nitro)benzenesulfonylamine derivative (3) are reacted to give compound (4). The resulting compound (4) is treated with thiophenol in the presence of a base such as potassium carbonate to eliminate the 2-nitrobenzenesulfonyl group, thereby giving amine compound (5). Alternatively, when R⁴ is H, it is possible to react compound (2) with potassium phthalimide and then treat the resulting phthalimide derivative (6) with hydrazine to give the corresponding amine compound (5).

On the other hand, compound (2) is reacted with ethyl isonipecotate (7) in a solvent such as acetonitrile, N,N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), tetrahydrofuran (THF), dioxane, toluene, benzene, etc. in the presence of a base such as potassium carbonate or the like at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature overnight, to give compound (8). The compound (8) is subjected to a usual alkaline hydrolysis to give the corresponding carboxylic acid compound (9).

The carboxylic acid compound (9) is reacted with the amine compound (5) using a dehydration condensing agent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (water-soluble carbodiimide), 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HBTU) or the like in a solvent such as chloroform, dichloroethane, THF, dioxane, acetonitrile, etc. at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 12 hours, to give an end product (1A).

Process B: Preparation of the compound of the formula (1) wherein l=1, m=0, n=1 and X=O

wherein, B, W¹, W², R¹, R² and R³ are as defined above, and J denotes a protecting group such as benzyloxycarbonyl, tert-butoxycarbonyl, acetyl, benzoyl or benzyl group. Incidentally, in the reaction schemes shown above and below, the expression “(W²→W¹)” following the term “compound(2)” means that W² in the formula representing compound (2) is changed to W¹.

4-hydroxypiperidine compound (10) with a protected amino group is reacted with compound (2) in the presence of sodium hydride or potassium iodide in a solvent such as DMF, DMSO, etc. at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 2 days, to give compound (11). The protecting group in the compound (11) is removed in a known manner. The resulting compound (12) is reacted with compound (2) in the presence of a base such as potassium carbonate in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane, etc. at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give an end product (1B).

Process C: Preparation of the compound of the formula (1) wherein l=1, m=0, n=0, X=NR⁴CO and R⁴=H or Me

wherein, B, W¹, W², R¹, R² and R³ are as defined above, and R⁴ denotes a hydrogen atom or methyl group.

Isonipecotamide (13) is reacted with compound (2) in the presence of a base such as potassium carbonate, sodium carbonate or the like in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane, etc. at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give compound (14). The compound (14) is subjected to Hofmann rearrangement reaction to give amine compound (15).

On the other hand, by subjecting the compound (14) to Hofmann rearrangement reaction in ethanol, carbamate compound (16) is obtained. Then, by subjecting the compound (16) to a reduction reaction using lithium aluminum hydride, methylamine compound (17) is obtained.

By reacting carboxylic acid compound (18) with the amine compound (15) or methylamine compound (17) similarly to the condensation reaction in Process A, an end compound (1C) is obtained.

Process D: Preparation of the compound of the formula (1) wherein l=1, m=0, n=1 and X=NR⁴

wherein B, W¹, W², R¹, R² and R³ are as defined above, and R⁴ denotes an alkyl alkenyl, alkynyl, aralkyl or heteroaralkyl group.

The amine compound (15) mentioned in the above is reacted with 2-nitrobenzenesulfonyl chloride (19) according to a known manner to give compound (20). The compound (20) is reacted with compound (2) in the presence of a base such as potassium carbonate in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane or the like at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give compound (21). The benzenesulfonyl group of the compound (21) is removed similarly to the procedure for the compound (4) in Process A to give an end compound (1D) (R⁴=H). The compound (1D) is reacted with R⁴—B in the presence of a base such as sodium carbonate, sodium bicarbonate, potassium carbonate, cesium carbonate or the like in a solvent such as acetonitrile, THF, dioxane, chloroform, dichloromethane, DMF, DMSO or the like at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at 80° C. for 12 hours, to give compound (1D′).

On the other hand, the methylamine compound (17) is reacted compound (2) in the presence of a base such as potassium carbonate in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane or the like at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give an end compound 1D″) (R⁴=Me).

Process E: Preparation of the compound of the formula (1) wherein l=1, m=0 or 1, n=1 and X=NR⁴,

wherein, B, J, W¹, W², R¹, R² and R³ are as defined above, and R⁴ denotes an alkyl, alkenyl, alkynyl, aralkyl or heteroaralkyl group.

Aminopiperidine derivative (22) in which the amino group on the ring is protected is reacted with compound (2) in the presence of a base such as potassium carbonate in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane or the like at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give compound (23). The compound (23) is reacted with R⁴—B in the presence of a base such as sodium carbonate, sodium bicarbonate, potassium carbonate, cesium carbonate or the like in a solvent such as acetonitrile, THF, dioxane, chloroform, dichloroethane, DMF, DMSO or the like at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at 80° C. for 12 hours, to give compound (24). After removal of the protecting group, the compound (25) is reacted compound (2) in the presence of a base such as potassium carbonate in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane or the like at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give compound (1E).

Process F: Preparation of the compound of the formula (1) wherein l=1, m=0, n=1 and X=NR⁴,

wherein, B, W¹, W², R¹, R² and R³ are as defined above, and R⁴ denotes an alkyl, alkenyl, alkynyl, aralkyl, heteroaralkyl, aryl or heteroaryl group.

4-piperidone ethylene ketal (26) is reacted with compound (2) in the presence of a base such as potassium carbonate in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane, etc. at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give compound (27), which in turn is deketalized by using an acid to give ketone compound (28).

On the other hand, 4-piperidone (29) is reacted compound (2) in the presence of a base such as potassium carbonate in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane or the like at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give compound (28). Using the compound (28), amine compound (30) can be prepared according to either of the following two synthesis processes:

Synthesis process 1: The compound (28) is reacted with an amine compound of the formula: R⁴—NH₂ in the presence of molecular sieves in toluene or benzene at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at reflux temperature for 12 hours, followed by reaction with a reducing agent such as sodium borohydride or sodium cyanoborohydride at a temperature between 0° C. and a reflux temperature for several minutes to several days, preferably at room temperature for 1 hour, to give the amine compound (30).

Synthesis process 2: The compound (28) is reacted with an amine compound of the formula: R⁴—NH₂ in the presence of a reducing agent such as sodium triacetoxy boron hydride in a solvent such as dichloromethane, 1,2-dichloroethane, methanol, ethanol, etc. at a temperature between 0° C. and a reflux temperature for several minutes to several days, preferably at room temperature for 4 hours, to give the amine compound (30).

The resulting compound (30) is reacted compound (2) in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane, etc. at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give an end product (IF).

Process G: Preparation of the compound of the formula (1) wherein l=1, m=0, n=1 and X=NR⁴

wherein, B, J, W, W², R¹, R² and R³ are as defined above, and R⁴ denotes an alkyl, alkenyl, alkynyl, aralkyl, heteroaralkyl, aryl or heteroaryl group.

4-piperidone derivative (31) in which the amino group on the ring is protected is reacted with an amine compound R⁴—NH₂ similarly to the procedure for preparation of compound (30) in Process F to give compound (32). The compound (32) is reacted with compound (2) in the presence of a base such as potassium carbonate in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane, etc. at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give compound (33). After removal of the protecting group from the compound (33), the resulting compound (34) is reacted with compound (2) in the presence of a base such as potassium carbonate in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane, etc. at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give an end product (1G).

Process H: Preparation of the compound of the formula (1) wherein l=0, m=0, n=1 and X=NH

wherein, B, J, W¹, W², R¹, R² and R³ are as defined above.

3-aminopyrrolidine derivative (35) with a protected amino group on the ring is reacted with 2-nitrobenzenesulfonyl chloride (19) under usual conditions to give a benzenesulfonyl derivative (36). The derivative (36) is reacted with compound (2) in the presence of a base such as potassium carbonate in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane, etc. at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give compound (37). The protecting group of the amino group is removed from the compound (37) to give compound (38), which in turn is reacted with compound (2) in the presence of a base such as potassium carbonate in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane, etc. at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give compound (39). By subjecting the compound (39) to a reaction similar to that in the preparation of compound (5) in Process A, an end product (1H) is obtained.

Process I: Preparation of the compound of the formula (1) wherein l=0, m=0, n=1 and X=NR⁴

wherein B, J, W¹, W², R¹, R², and R³ are as defined above, and R⁴ denotes an alkyl, alkenyl, alkynyl or aralkyl group.

Compound (36) is reacted with R⁴—B in the presence of a base such as sodium carbonate, potassium carbonate, etc. in a solvent such as acetonitrile, THF, dioxane, chloroform, dichloroethane, DMF, DMSO, etc. at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at 80° C. for 12 hours, to give compound (40). The amino-protecting group is removed from the compound (40), and the resulting compound (41) is reacted with compound (2) in the presence of a base such as potassium carbonate in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane, etc. at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give compound (42). By subjecting the compound (42) to a reaction similar to that in the preparation of compound (5) in Process A, compound (43) is obtained. The compound (43) is reacted with compound (2) in the presence of a base such as potassium carbonate in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane, etc. at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give an end product (1I).

Process J: Preparation of the compound of the formula (1) wherein R²=OH

wherein, X, W¹, W², R, R³, l, m and n have the same meanings as initially defined.

By reacting methoxy compound (1J) with iodotrimethylsilane in a solvent such as toluene, chloroform, dichloromethane, etc. at a temperature between −25° C. and a reflux temperature for several minutes to several days, preferably at 0° C. for 2 hours, there can be obtained an end product (1J′).

Process K: Preparation of the compound of the formula (1) wherein l=1, m=0, n=0 and X=NR⁴CO

wherein, B, J, W¹, W², R¹, R² and R³ are as defined above, and R⁴ denotes an alkyl, alkenyl, alkynyl, aralkyl, heteroaralkyl, aryl or heteroaryl group.

Compound (32), which is described in the Process G, is reacted with compound (18) in the similar procedure as described in the preparation of compound (1A) in Process A to give gompound (44). After removal of the protecting group from the compound (44), the resulting compound (45) is reacted with compound (2) in the presence of a base such as potassium carbonate in a solvent such as acetonitrile, DMF, DMSO, THF, dioxane, etc. at a temperature between 0° C. and a reflux temperature for several hours to several days, preferably at room temperature for 4 hours, to give an end product (1K).

The compounds (1) according to the present invention are obtained by any of the above-described processes and may further be purified by using an ordinary purification means such as recrystallization or column chromatography as needed. As needed, the compounds may also be converted into the desired salts or solvates in a method known per se in the art. When the compounds (1) have an asymmetric carbon atom, the present invention includes any configurational isomers.

The compounds (1) according to the present invention, or salts or solvates thereof thus obtained have an excellent inhibitory effect on cell adhesion as demonstrated in the examples, which will be described subsequently, and are useful as medicines for treatment and prevention of diseases of animals including humans, caused by cell adhesion or cell infiltration, for example, asthma, allergy, rheumatism, arteriosclerosis, inflammation, Sjogren's syndrome, etc.

The medicine according to the present invention comprises a compound (1), a salt thereof, or a solvate thereof as an active ingredient. The form of administration may be suitably selected as necessary for the therapeutic application intended without any particular limitation, including oral preparations, injections, suppositories, ointments, inhalants, eye drops, nose drops and plasters. A composition suitable for use in these administration forms can be prepared by blending a pharmaceutically acceptable carrier in accordance with the conventional preparation method publicly known by those skilled in the art.

When an oral solid preparation is formulated, an excipient, and optionally, a binder, disintegrator, lubricant, colorant, a taste corrigent, a smell corrigent and the like are added to compound (1) and the resulting composition can be formulated into tablets, coated tablets, granules, powders, capsules, etc. in accordance with methods known in the art.

As such additives described above, any additives may be used which are generally used in the pharmaceutical field. Examples include excipients such as lactose, sucrose, sodium chloride, glucose, starch, calcium carbonate, kaolin, microcrystalline cellulose and silicic acid; binders such as water, ethanol, propanol, simple syrup, glucose solution, starch solution, gelatin solution, carboxymethyl cellulose, hydroxypropyl cellulose, hydroxypropyl starch, methyl cellulose, ethyl cellulose, shellac, calcium phosphate and polyvinyl pyrrolidone; disintegrators such as dry starch, sodium alginate, agar powder, sodium hydrogencarbonate, calcium carbonate, sodium lauryl sulfate, monoglyceryl stearate and lactose; lubricants such as purified talc, stearic acid salts, borax and polyethylene glycol; and taste corrigents such as sucrose, orange peel, citric acid and tartaric acid.

When an oral liquid preparation is formulated, a taste corrigent, buffer, stabilizer, smell corrigent and/or the like are added to compound (1) and the resulting composition can be formulated into internal liquid preparations, syrup preparations, elixirs, etc. in accordance with methods known in the art. In this case, vanillin as the taste corrigent, may be used. As the buffer, sodium citrate may be mentioned. As examples of the stabilizer, tragacanth, gum arabic and gelatin may be mentioned.

When an injection is formulated, a pH adjustor, buffer, stabilizer, isotonicity agent, local anesthetic and the like may be added to compound (1) according to the present invention, and the resultant composition can be formulated into subcutaneous, intramuscular and intravenous injections in accordance with methods known in the art. Examples of the pH adjustor and buffer in this case include sodium citrate, sodium acetate and sodium phosphate. Examples of the stabilizer include sodium pyrosulfite, EDTA, thioglycolic acid and thiolactic acid. Examples of the local anesthetic include procaine hydrochloride and lidocaine hydrochloride. Examples of the isotonicity agent include sodium chloride and glucose.

When a suppository is formulated, a carrier preparation known in the art, for example, polyethylene glycol, lanoline, cacao butter, fatty acid triglyceride or the like, and optionally, a surfactant such as Tween (trade mark) and the like are added to the compound (1), and the resultant composition can be formulated into suppositories in accordance with methods known in the art.

When an ointment is formulated, a base material, stabilizer, wetting agent, preservative and the like, which are generally used, are blended with compound (1) as needed, and the resulting blend is mixed and formulated into ointments in accordance with known method known methods. Examples of the base material include liquid paraffin, white vaseline, bleached beeswax, octyldodecyl alcohol and paraffin. Examples of the preservative include methyl p-hydroxybenzoate, ethyl p-hydroxybenzoate and propyl p-hydroxybenzoate.

Besides the above preparations, inhalants, eye drops and nose drops may also be formulated in accordance with known methods.

The dose of the medicine according to the present invention varies according to the age, weight and condition of the patient to be treated, the administration method, the number of times of administration, and the like. It is however preferred that the medicine is generally orally or parenterally administered at once or in several portions in a dose of 1 to 1,000 mg per day in terms of compound (1), for an adult.

The present invention will hereinafter be described in more detail by Examples. However, the present invention is not limited to these examples.

PREPARATION EXAMPLE 1 Synthesis of Ethyl 2-(3,4,5-Trimethoxyphenyl)isonicotinate

3,4,5-Trimethoxyphenylboronic acid (20.10 g) and ethyl 2-chloroisonicotinate (18.56 g) were suspended in a mixted solvent of toluene (200 mL) and THF (100 mL), and to the suspension 2 M sodium carbonate (200 mL) and tetrakis(triphenyl phosphine) palladium(0) (5.78 g) were added. The mixture was stirred at 90° C. overnight under an argon atmosphere. Ethyl acetate was added to the reaction mixture to separate an organic layer. The organic layer was washed with brine, dried over anhydrous sodium magnesium and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using hexane-ethyl acetate (5:1) to give the title compound.

Yield: 27.99 g (88%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (t, 3H, J=7.0 Hz), 3.92 (s, 3H), 3.99 (s, 6H), 4.46 (q, 2H, J=7.0 Hz), 7.30 (s, 2H), 7.76 (dd, 1H, J=5.1 Hz, 1.6 Hz), 8.24 (dd, 1H, J=1.6 Hz, 0.8 Hz), 8.81 (dd, 1H, J=5.1 Hz, 0.8 Hz).

PREPARATION EXAMPLE 2 Synthesis of 4-Hydroxymethyl-2-(3,4,5-trimethoxyphenyl)pyridine

Ethyl 2-(3,4,5-trimethoxyphenyl)isonicotinate (24.57 g) was dissolved in dry THF (200 mL), and to the solution lithium aluminum hydride (2.94 g) was added at 0° C. under an argon atmosphere. The mixture was stirred at 0° C. for 1 hour as it is. A small amount of water and then sodium sulfate were added to the reaction mixture, and the reaction mixture was filtered through celite. The filtrate was evaporated, and the reultant crude crystals were recrystalized from ethyl acetate-hexane to give the title compound.

Yield: 17.53 g (82%). ¹H-NMR (400 MHz, CDCl₃) δ: 3.90 (s, 3H), 3.95 (s, 6H), 4.79 (s, 2H), 7.19 (d, 1H, J=5.1 Hz), 7.21 (s, 2H), 7.66 (s, 1H), 8.60 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 3 Synthesis of 4-Chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine

4-hydroxymethyl-2-(3,4,5-trimethoxyphenyl)pyridine (19.18 g) was dissolved in chloroform (100 mL), and to the solution thinly chloride (10.2 mL) was added at 0° C. After 30 minutes, the mixture was warmed to room temperature and stirred for 4 hours. The reaction mixture was washed with aqaueous saturated sodium hydrogendcarbonate and brine, dried over anhydrous sodium sulfate and evaporated. The residue was then recrystallized from ethyl acetate-hexane to give the title compound as pale yellow crystalline powder.

Yield: 18.24 g (89%). ¹H-NMR (400 MHz, CDCl₃) δ: 3.91 (s, 3H), 3.97 (s, 6H), 4.61 (s, 2H), 7.24 (s, 2H), 7.26 (d, 1H, J=5.1 Hz), 7.68 (s, 1H), 8.67 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 4 Synthesis of N-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]phthalimide

To a solution of 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (881 mg) in chloroform (10 mL) was added potassium phthalimide (556 mg). The mixture was stirred at room temperature overnight and water was added. After separating the organic layer, the aqueous layer was extracted with chloroform. Organic layers were combined, dried over anhydrous magnesium sulfate and evaporated to give the title compound as white powder.

Yield: 1.16 g (96%).

PREPARATION EXAMPLE 5 Synthesis of 4-Aminomethyl-2-(3,4,5-trimethoxyphenyl)pyridine

To a suspension of N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]phthalimide (1.16 g) in ethanol (30 mL) was added hydrazine monohydrate (1 mL). The mixture was refluxed for 3 hours. After cooling, the precipitates were filtered off. The filtrate was evaporated and the residue was dissolved in chloroform. The solution was washed with saturated aqueous sodium hydrogen carbonate and brine, dried over anhydrous magnesium sulfate and evaporated to give the title compound as pale yellow oil.

Yield: 418 mg (53%).

PREPARATION EXAMPLE 6 Synthesis of Ethyl 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]piperidine-4-carboxylate

To a solution of ethyl piperidine-4-carboxylate (514 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (969 mg) in acetonitrile (20 mL) was added potassium carbonate (452 mg). The mixture was stirred at room temperature for 4 hours and evaporated. The residual oil was subjected to a column of silica gel and eluted using hexane-ethyl acetate (2:1) and then chloroform-methanol (40:1). Fractions containing the product were collected and evaporated to give the title compound as white prisms.

Yield: 1.20 g (88%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.25 (t, 3H, J=7.0 Hz), 1.72-1.93 (m, 4H), 2.10 (t, 2H, J=9.8 Hz), 2.27-2.35 (m, 1H), 2.86 (d, 2H, J=11.3 Hz), 3.55 (s, 2H), 3.91 (s, 3H), 3.98 (s, 6H), 4.14 (q, 2H, J=7.0 Hz), 7.21 (d, 1H, J=4.9 Hz), 7.24 (s, 2H), 7.63 (s, 1H), 8.59 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 7 Synthesis of 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]piperidine-4-carboxylic Acid

To a solution of ethyl 1-[[2-(3,4,5-trimethoxyphenyl)prydine-4-yl]methyl]piperidine-4-carboxylate (760 mg) in ethanol (10 mL) was added 1 M sodium hydroxide (10 mL). The mixture was stirred at room temperature for 4 hours and evaporated. The residue was dissolved in water (20 mL) and 5% aqueous potassium hydrogen sulfate was added dropwise until pH of the solution became 7. Precipitates were collected and the product was used for the next steps without further purification.

Yield: 779 mg (theoretical amount).

EXAMPLE 1

 

Synthesis of 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methylaminocarbonyl]piperidine Maleate

To a solution of 1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine-4-caroxylic acid (97 mg) and 4-aminomethyl-2-(3,4,5-trimethoxyphenyl)pyridine (68 mg) in acetonitrile (5 mL) was added HBTU (95 mg). The mixture was stirred at room temperature for 12 hours and evaporated. The residual oil was dissolved in chloroform, washed with saturated aqueous sodium hydrogen carbonate and brine, dried over anhydrous magnesium sulfate and evaporated. Resulting residue was applied to a column of silica gel and eluted using chloroform-methanol (40:1) and then chloroform-methanol (20:1). Fractions containing the product were collected and evaporated. The free base of the product was then converted to a maleate by the usual method.

Yield: 93 mg (49%). ¹H-NMR (400 MHz, measured as a maleate, DMSO-d₆) δ: 1.87-2.01 (m, 4H), 2.48-2.56 (m, 1H), 2.78-2.86 (m, 2H), 3.26-3.31 (m, 2H), 3.78 (s, 3H), 3.79 (s, 3H), 3.87 (s, 6H), 3.90 (s, 6H), 4.15 (s, 2H), 4.39 (d, 2H, J=5.9 Hz), 6.16 (s, 2H), 7.16 (d, 1H, J=5.9 Hz), 7.35 (s, 2H), 7.39 (d, 1H, J=5.9 Hz), 7.39 (s, 2H), 7.73 (s, 1H), 7.95 (s, 1H), 8.15 (d, 1H, J=5.9 Hz), 8.54 (d, 1H, J=4.9 Hz), 8.68 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 8 Synthesis of 1-(Benzyloxycarbonyl)-4-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyloxy]piperidine

To a solution of 1-(benzyloxycarbonyl)-4-hydroxypiperidine (1.00 g) in DMF (20 mL) was added sodium hydride (55% dispersion in mineral oil, 222 mg). The mixture was stirred at room temperature for 1 hour and then, 4-chlolromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (1.37 g) and potassium iodide (755 mg) was added. The mixture was stirred at 70° C. overnight, poured into water and extracted with chloroform. The organic layer was washed with brine, dried over anhydrous sodium sulfate and evaporated. The residual oil was applied to a column of silica gel and column chromatography was performed using chloroform-methanol (99:1) as an eluent giving the title compound.

Yield: 213 mg (10%). ¹H NMR (400 MHz, CDCl₃) δ: 1.63 (br, 2H), 1.89 (br, 2H), 3.20-3.35 (m, 2H), 3.57-3.68 (m, 1H), 3.84-3.92 (m, 5H), 3.94 (s, 6H), 4.62 (s, 2H), 5.11 (s, 2H), 7.21-7.35 (m, 8H), 7.61 (s, 1H), 8.61 (d, 1H, J=5.0 Hz).

PREPARATION EXAMPLE 9 Synthesis of 4-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyloxy]piperidine

To a solution of 1-(benzyloxycarbonyl)-4-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyloxy]piperidine (213 mg) in methanol (10 mL) was added 40% aqueous potassium hydroxide (10 mL). The mixture was stirred at 100° C. for 3 hours and evaporated. Water was added to the residue and extracted with chloroform. The organic layer was washed with brine, dried over anhydrous sodium sulfate and evaporated. The residual oil was subjected to column chromatography of silica gel using chloroform-ammonia saturated methanol (20:1) to give the title compound.

Yield: 93 mg (60%). ¹H NMR (400 MHz, CDCl₃) δ: 1.55-1.68 (m, 2H), 2.01 (br, 2H), 2.67-2.72 (m, 2H), 3.13-3.18 (m, 2H), 3.50-3.60 (m, 1H), 3.91 (s, 3H), 3.97 (s, 6H), 4.64 (s, 2H), 7.22 (d, 1H, J=4.3 Hz), 7.24 (s, 2H), 7.64 (s, 1H), 8.63 (d, 1H, J=5.1 Hz).

EXAMPLE 2

 

Synthesis of 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyloxy]piperidine Trihydrochloride

4-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyloxy]piperidine (70 mg), 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (22 mg), potassium carbonate (56 mg) and potassium iodide (40 mg) were suspended in acetonitrile (5 mL). The mixture was stirred at room temperature for 5 hr and evaporated. Chloroform and water were added to the residual oil and the organic layer was separated. Aqueous layer was then extracted with chloroform and the organic layers were combined, dried over anhydrous magnesium sulfate and evaporated. The residue was applied to a column of silica gel using chloroform-methanol (40:1) as an eluent. Fractions containing the product were collected and evaporated. The title compound was obtained by converting the free base to a trihydrochloride.

Yield: 42 mg (39%). ¹H NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.53-2.42 (m, 6H), 2.80 (br, 2H), 3.57 (br, 3H), 3.88 (s, 6H), 3.94 (s, 6H), 3.95 (s, 6H), 4.60 (s, 2H), 7.18-7.24 (m, 6H), 7.61 (s, 2H), 8.58-8.61 (m, 2H).

PREPARATION EXAMPLE 10 Synthesis of (3S)-1-(tert-Butoxycarbonyl)-3-[(2-nitrobenzene)sulfonylamino]pyrrolidine

To an ice-cooled solution of(3S)-3-amino-1-(tert-butoxycarbonyl)pyrrolidine (404 mg) and triethylamine (220 mg) in THF (5 mL) was added 2-nitrobenzenesulfonyl chloride (481 mg). The mixture was stirred at room temperature for 30 minutes and evaporated. Ethyl acetate was added to the residue. The solution was washed with water and brine, dried over anhydrous sodium sulfate and evaporated. The residual oil was subjected to a column of silica gel and column chromatography was performed using chroloform-methanol (20:1) as an eluent. Fractions containing the product were collected and evaporated to give the title compound as pale yellow amorphous.

Yield: 597 mg (74%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.44 (s, 9H), 1.80-2.12 (m, 2H), 3.14-3.44 (m, 4H), 4.02 (br, 1H), 5.48 (d, 1H, J=7.2 Hz), 7.77 (t, 2H, J=4.4 Hz), 7.87-7.90 (m, 1H), 8.17-8.19 (m, 1H).

PREPARATION EXAMPLE 11 Synthesis of (3S)-1-(tert-Butoxycarbonyl)-3-[N-methyl-N-(2-nitrobenzene)sulfonylamino]pyrrolidine

To a suspension of (3S)-1-(tert-butoxycarbonyl)-3-[(2-nitrobenzene)sulfonylamino]pyrrolidine (371 mg) and potassium carbonate (141 mg) in acetonitrile (10 mL) was added methyl iodide (141 mg). The mixture was stirred at 60° C. for 2 hours and evaporated. Ethyl acetate was added to the mixture. The solution was washed with saturated aqueous sodium hydrogen carbonate and brine, dried over anhydrous sodium sulfate and evaporated. The residue was applied to a column of silica gel using hexane-ethyl acetate (2:1) as an eluent. Fractions containing the product were collected and evaporated to give the title compound as yellow syrup.

Yield: 365 mg (95%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.44 (s, 9H), 1.95 (br, 1H), 2.09 (br, 1H), 2.87 (s, 3H), 3.20-3.31 (m, 2H), 3.53 (br, 2H), 4.58 (br, 1H), 7.65 (br, 1H), 7.71 (br, 2H), 8.04 (br, 1H).

PREPARATION EXAMPLE 12 Synthesis of (3S)-3-[N-Methyl-N-(2-nitrobenzene)sulfonylaminol]pyrrolidine

To an ice-cooled solution of (3S)-1-(tert-butoxycarbonyl)-3-[N-methyl-N-(2-nitrobenzenesulfonyl)amino]pyrrolidine (365 mg) in dichloromethane (25 mL) was added trifluoroacetic acid (1 mL). The mixture was stirred at room temperature for 3 hours and evaporated. The residue was dissolved in chloroform. The solution was washed with saturated aqueous sodium hydrogen carbonate and brine, dried over anhydrous sodium sulfate and evaporated to give the title compound as yellow syrup.

Yield: 135 mg (50%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.69-1.74 (m, 1H), 1.87 (br, 1H), 1.95-2.02 (m, 1H), 2.80 (dd, 1H, J=11.7 Hz, 5.7 Hz), 2.84-2.91 (m, 4H), 2.96-3.05 (m, 1H), 3.10 (dd, 1H, J=11.7 Hz, 8.2 Hz), 4.48-4.56 (m, 1H), 7.61-7.63 (m, 1H), 7.66-7.73 (m, 2H), 8.01-8.04 (m, 1H).

PREPARATION EXAMPLE 13 Synthesis of (3S)-3-[N-Methyl-N-(2-nitrobenzene)sulfonylamino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]pyrrolidine

(3S)-3-[N-methyl-N-(2-nitrobenzene)sulfonylaminol]pyrrolidine (135 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (139 mg) were coupled in the same manner as described in Example 2 to give the title compound as yellow amorphous.

Yield: 247 mg (96%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.80-1.87 (m, 1H), 2.15-2.30 (m, 2H), 2.52 (dd, 1H, J=10.5 Hz, 8.2 Hz), 2.71 (dd, 1H, J=10.5 Hz, 8.2 Hz), 2.90 (dt, 1H, J=8.8 Hz, 2.9 Hz), 2.96 (s, 3H), 3.53 (d, 1H, J=13.9 Hz), 3.68 (d, 1H, J=13.9 Hz), 3.90 (s, 3H), 3.96 (s, 6H), 4.61-4.68 (m, 1H), 7.16 (dd, 1H, J=4.9 Hz, 1.2 Hz), 7.21 (s, 2H), 7.58-7.60 (m, 2H), 7.64-7.69 (m, 2H), 7.99-8.02 (m, 1H), 8.58 (d, 1H, J=4.9 Hz,).

PREPARATION EXAMPLE 14 Synthesis of (3S)-3-Methylamino-1-[[2-(3,4,5-trimethoxyphenyl)-pyridin-4-yl]methyl]pyrrolidine

To a solution of (3S)-3-[N-methyl-N-(2-nitrobenzene)sulfonylamino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]pyrrolidine (242 mg) in acetonitrile (5 mL) was added potassium carbonate (94 mg) and thiophenol (75 mg). The mixture was stirred at 80° C. for 3 hours and evaporated. Ethyl acetate was added to the mixture, the solution was washed with saturated aqueous sodium hydrogen carbonate, water, and bine, dried over anhydrous sodium sulfate and evaporated. The residual oil was subjected to preparative TLC using chloroform-methanol (20:1) as a solvent system giving yellow syrup of the title compound.

Yield: 104 mg (64%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.32 (br, 1H), 1.56-1.64 (m, 1H), 2.11-2.17 (m, 1H), 2.38 (s, 3H), 2.44 (dd, 1H, J=7.4 Hz, 4.5 Hz), 2.50-2.55 (m, 1H), 2.66-2.75 (m, 2H), 3.20-3.26 (m, 1H), 3.66 (s, 2H), 3.90 (s, 3H), 3.97 (s, 6H), 7.21 (d, 1H, J=4.1 Hz), 7.25 (s, 2H), 7.64 (s, 1H), 8.59 (d, 1H, J=4.9 Hz).

EXAMPLE 3

 

Synthesis of (3S)-3-[N-Methyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-yl]methyl]pirrolidine Tertrahydrochloride

(3S)-3-methylamino-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]pyrrolidine (104 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (85 mg) was condensed in the same manner as described in Example 2. Yellow syrup obtained was converted to a tetrahydrochloride by the usual method giving the title compound as yellow powder.

Yield: 151 mg (68%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.89-1.92 (m, 1H), 2.04-2.08 (m, 1H), 2.18 (s, 3H), 2.60-2.76 (m, 4H), 3.25-3.29 (m, 1H), 3.53 (d, 1H, J=14.3 Hz), 3.62 (d, 1H, J=14.3 Hz), 3.64 (d, 1H, J=13.9 Hz), 3.73 (d, 1H, J=13.9 Hz), 3.89 (s, 6H), 3.95 (s, 6H), 3.96 (s, 6H), 7.20-7.21 (m, 2H), 7.23 (s, 2H), 7.24 (s, 2H), 7.61 (s, 1H), 7.65 (s, 1H), 8.59 (d, 1H, J=5.7 Hz), 8.60 (d, 1H, J=5.3 Hz).

PREPARATION EXAMPLE 15 Synthesis of 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]piperidine-4-carboxamide

Piperidine-4-carboxamide (385 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (881 mg) were condensed by the same method as described in Example 2 to give the title compound as white needles.

Yield: 1.01 g (87%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.70-1.88 (m, 4H), 2.01-2.23 (m, 3H), 2.95 (d, 2H, J=11.0 Hz), 3.56 (s, 2H), 3.90 (s, 3H), 3.98 (s, 6H), 5.46 (d, 2H, J=16.3 Hz), 7.21 (d, 1H, J=5.0 Hz), 7.24 (s, 2H), 7.64 (s, 1H), 8.59 (d, 1H, J=5.0 Hz).

PREPARATION EXAMPLE 16 Synthesis of 4-Amino-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

To a solution of 1-[[2-(3,4,5-trimethoxypheyl)pyridin-4-yl]methyl]piperidine-4-carboxamide (192 mg) in a mixed solvent of water (50 mL) and acetonitrile (50 mL) was added [bis(trifluoroacetoxy)iodo]benzene (323 mg). The mixture was stirred at room temperature overnight and evaporated. Saturated aqueous sodium hydrogen carbonate was added to the residue and extracted with chloroform. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and evaporated. Yellow syrup obtained was then converted to trihydrochloride which gave yellow powder. The title compound was used for next step without further purification.

Yield: 201 mg (theoretical amount).

PREPARATION EXAMPLE 17 Synthesis of 2-(3,4,5-Trimethoxyphenyl)isonicotinic Acid

To a solution of ethyl 2-(3,4,5-trimethoxyphenyl)isonicotinate (3.17 g) in ethanol (40 mL) was added 10% potassium hydroxide (2.42 g). The mixture was stirred at room temperature for 5 hours and evaporated. Water was added to the residue and pH was adjusted to 7. White precipitates of the title compound were collected by filtration and the compound was used for next step without further purification.

Yield: 2.60 g (90%).

EXAMPLE 4

 

Synthiesis of 4-[2-(3,4,5-Trimethoxyphenyl)pyridin-4-carbonylamino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Maleate

2-(3,4,5-trimethoxyphenyl)isonicotinic acid (72 mg) and 4-amino-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (117 mg) were condensed in the same manner as described in Example 1. The title compound was obtained as a maleate.

Yield: 173 mg (93%). ¹H-NMR (400 MHz, measured as a maleate, DMSO-d₆) δ: 1.82-1.94 (m, 2H), 2.03-2.08 (m, 2H), 2.77-2.83 (m, 2H), 3.20-3.27 (m, 2H), 3.79 (s, 6H), 3.90 (s, 12H), 4.00 (br, 1H), 4.06 (s, 2H), 6.15 (s, 2H), 7.36-7.38 (m, 1H), 7.39 (s, 2H), 7.41 (s, 2H), 7.61-7.63 (m, 1H), 7.90 (s, 1H), 8.12 (s, 1H), 8.27-8.32 (m, 1H), 8.67 (d, 1H, J=4.9 Hz), 8.74 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 18 Synthesis of 4-[(2-Nitrobenzene)sulfonylamino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine

4-amino-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (467 mg) and 2-nitrobenzenesulfonyl chloride (244 mg) were condensed in the same manner as described in Preparation Example 10 to give the title compound.

Yield: 494 mg (91%).

PREPARATION EXAMPLE 19 Synthesis of 4-[N-(2-Nitrobenzene)sulfonyl-N-[[2-(3,4,5-trimethoxyphenyl)-pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine

4-[(2-nitrobenzene)sulfonylamino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (494 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (267 mg) were condensed in the same manner as described in Example 2 to give the title compound.

Yield: 443 mg (61%).

EXAMPLE 5

 

Synthesis of 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methylamino]piperidine Difumalate

4-[N-(2-nitrobenzene)sulfonyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (443 mg) was treated in the same manner as described in Preparation Example 14. The title compound was obtained after converting to a difumalate.

Yield: 103 mg (24%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.44-1.53 (m, 2H), 1.87-1.91 (m, 2H), 2.15 (t, 2H, J=1.1 Hz), 2.57-2.64 (m, 1H), 2.82-2.85 (m, 2H), 3.59 (s, 2H), 3.78 (s, 6H), 3.89 (s, 12H), 3.90 (s, 2H), 6.63 (s, 4H), 7.24 (d, 1H, J=4.9 Hz), 7.29 (d, 1H, J=4.9 Hz), 7.35 (s, 2H), 7.37 (s, 2H), 7.76 (s, 1H), 7.85 (s, 1H), 8.53-8.56 (m, 2H).

PREPARATION EXAMPLE 20 Synthesis of 4-(Ethoxycarbonylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine

To a solution of 1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine-4-carboxamide (528 mg) in a mixed solvent of ethanol (10 mL) and acetonitrile (10 mL) was added [bis(trifluoroacetoxy)iodo]benzene (884 mg). The mixture was stirred at room temperature overnight and evaporated. Saturated aqueous sodium hydrogen carbonate was added to the residue and extracted with chloroform. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and evaporated. The residue was applied to a column of silica gel and purified using chloroform-methanol (20:1) as an eluent to give the title compound.

Yield: 566 mg (96%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.21 (t, 3H, J=7.0 Hz), 1.40-1.51 (m, 2H), 1.92 (d, 2H, J=10.9 Hz), 2.15 (t, 2H, J=10.9 Hz), 2.78 (d, 2H, J=11.6 Hz), 3.52 (br, 3H), 3.87 (s, 3H), 3.94 (s, 6H), 4.07 (q, 2H, J=7.0 Hz), 4.56 (br, 1H), 7.17 (d, 1H, J=4.9 Hz), 7.21 (s, 2H), 7.59 (s, 1H), 8.56 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 21 Synthesis of 4-(Methylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine

To a suspension of lithium aluminum hydride (100 mg) in dry THF (50 mL) was added a solution of 4-(ethoxycarbonylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (566 mg) in dry THF (50 mL) under an argon atmosphere. The mixture was then refluxed overnight, then cooled down. Saturated aqueous ammonium chloride was added to the mixture and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and evaporated. The residue was subjected to silica gel column chromatography using chloroform-ammonia saturated methanol (9:1) to give the title compound as yellow oil.

Yield: 379 mg (78%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.36-1.46 (m, 2H), 1.89 (d, 2H, J=12.5 Hz), 2.10 (dt, 2H, J=11.5 Hz, 1.1 Hz), 2.35-2.43 (m, 1H), 2.43 (s, 3H), 2.86 (d, 2H, J=11.6 Hz), 3.56 (s, 2H), 3.90 (s, 3H), 3.97 (s, 6H), 7.21 (d, 1H, J=5.1 Hz), 7.24 (s, 2H), 7.64 (s, 1H), 8.59 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 22 Synthesis of 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone Ethylene Ketal

4-Piperidone ethylene ketal (12.0 g) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (12.3 g) was condensed in the same manner as described in Example 2 to give the title compound.

Yield: 19.0 g (theoretical amount). ¹H-NMR (400 MHz, CDCl₃) δ: 1.68 (t, 4H, J=5.6 Hz), 2.48 (br, 4H), 3.50 (s, 2H), 3.82 (s, 3H), 3.86 (s, 4H), 3.88 (s, 6H), 7.13 (d, 1H, J=4.9 Hz), 7.17 (s, 2H), 7.57 (s, 1H), 8.5.1 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 23 Synthesis of 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone

To a solution of 1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone ethylene ketal (19.0 g) in THF (200 mL) was added 1 M hydrochloric acid (200 mL). The mixture was stirred at 90° C. overnight, then neutralized with 2 M sodium hydroxide and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and evaporated. The residual oil was applied to a column of silica gel using chloroform-methanol (40:1) as an eluent. Fractions containing the product were collected and evaporated to give the title compound.

Yield: 15.0 g (75%). ¹H-NMR (400 MHz, CDCl₃) δ: 2.48 (t, 4H, J=6.1 Hz), 2.79 (t, 4H, J=6.0 Hz), 3.69 (s, 2H), 3.89 (s, 3H), 3.96 (s, 6H), 7.24 (s, 2H), 7.26 (d, 1H, J=4.9 Hz), 7.66 (s, 1H), 8.62 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 24 Synthesis of 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone

4-Piperidone hydrochloride monohydrate (3.07 g) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (2.94 g) were coupled by the same manner as described in Example 2 to give the title compound.

Yield: 3.55 g (99%).

PREPARATION EXAMPLE 25 Synthesis of 4-(Methylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine

To a solution of 1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone (1.00 g) in 1,2-dichloroethane (60 mL) was added 30% solution of methylamine in ethanol (750 mg) and sodium triacetoxyborohydride (1.66 g). The mixture was stirred at room temperature for 3 hours, then small amount of water was added and evaporated. Water was added to the residue and extracted with chloroform. The organic layer was washed with brine, dried over anhydrous sodium sulfate and evaporated. The residue was subjected to silica gel column chromatography using chloroform-methanol (40:1) to give the title compound.

Yield: 640 mg (62%).

PREPARATION EXAMPLE 26 Synthesis of Ethyl 3-(3,4,5-Trimethoxyphenyl)benzoate

3,4,5-Trimethoyphenylboronic acid (3.7 g) and ethyl 3-bromobenzoate (4.02 g) were condensed in the same manner as described in Preparation Example 1 to give the title compound.

Yield: 5.09 g (92%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.42 (t, 3H, J=7.1 Hz), 3.90 (s, 3H), 3.94 (s, 6H), 4.41 (q, 2H, J=7.1 Hz), 6.79 (s, 2H), 7.50 (t, 1H, J=7.8 Hz), 7.73 (dt, 1H, J=7.1 Hz, 1.5 Hz), 8.01 (dt, 1H, J=7.8 Hz, 1.4 Hz), 8.23 (t, 1H, J=1.8 Hz).

PREPARATION EXAMPLE 27 Synthesis of 3-(3,4,5-Trimethoxyphenyl)benzoic Acid

Ethyl 3-(3,4,5-trimethoxyphenyl)benzoate (1.19 g) was treated in the same manner as described in Preparation Example 17 to give the title compound.

Yield: 986 mg (91%).

EXAMPLE 6

 

Synthesis of 4-[N-Methyl-N-[3-(3,4,5-trimethoxyphenyl)]benzoylamino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

3-(3,4,5-trimethoxyphenyl)benzoic acid (1.03 g) and 4-(methylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (1.32 g) were condensed in the same method as described in Example 1. The title compound was obtained after converting a free amine to a dihydrochloride.

Yield: 1.44 g (57%). ¹H-NMR (400 MHz, measured as a dihydrochloride, DMSO-d₆) δ: 1.89 (d, 2H, J=11.7 Hz), 2.54-2.62 (m, 2H), 2.89 (s, 3H), 3.09 (t, 2H, J=12.7 Hz), 3.43 (d, 2H, J=14.4 Hz), 3.76 (s, 3H), 3.78 (s, 3H), 3.88 (s, 6H), 3.91 (s, 6H), 4.34 (br, 3H), 6.91 (s, 2H), 7.33 (d, 1H, J=7.6 Hz), 7.47-7.51 (m, 2H), 7.54 (s, 2H), 7.60 (s, 1H), 7.71 (d, 1H, J=7.8 Hz), 8.55 (s, 1H), 8.68 (d, 1H, J=5.1 Hz).

EXAMPLE 7

 

Synthesis of 4-[N-Methyl-N-[[5-(3,4,5-trimethoxyphenyl)pyridin-3-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Difumarate

4-methylamino-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (135 mg) and 3-chloromethyl-5-(3,4,5-trimethoxypyenyl)pyridine (107 mg) were condensed by the same method as described in Example 2. White powder of the title compound was obtained after converting a free base to a difumarate.

Yield: 180 mg (58%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.69-1.73 (m, 2H), 1.82-1.85 (m, 2H), 2.03-2.08 (m, 2H), 2.25 (s, 3H), 2.48-2.51 (m, 1H), 2.97-2.99 (m, 2H), 3.56 (s, 2H), 3.67 (s, 2H), 3.90 (s, 3H), 3.91 (s, 3H), 3.94 (s, 6H), 3.98 (s, 6H), 6.76 (s, 2H), 7.22 (d, 1H, J=5.1 Hz), 7.24 (s, 2H), 7.62 (s, 1H), 7.80 (s, 1H), 8.50 (d, 1H, J=2.0 Hz), 8.60 (d, 1H, J=4.3 Hz), 8.69 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 28 Synthesis of 1-Bromo-4-chloro-3,5-dimethoxybenzene

A solution of sodium nitrite (97 mg) in water (2.0 mL) was added dropwise to an ice-cold suspension of 4-bromo-2,6-dimethoxyaniline (232 mg) in 6.0 M hydrochloric acid (2.5 mL). After stirring in ice for 30 minutes, a solution of cupric chloride (495 mg) in concentrated hydrochloric acid (2.0 mL) was added. The reaction mixture was stirred at room temperature for 30 minutes, then at 100° C. for 2 hours, and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium hydrogencarbonate and water, dried over anhydrous sodium sulfate, and evaporated. The residue was subjected to a column of silica gel using hexane-ethyl acetate (10:1) as an eluent to give the title compound as white powder.

Yield: 230 mg (92%).

PREPARATION EXAMPLE 29 Synthesis of 4-Chloro-3,5-dimethoxyphenylboronic Acid

Under an argon atomsphere, to dry THF (2 mL) stirred in a dry ice-methanol bath was gradually added a 1.57 M solution of n-butyllithium in hexane (0.8 mL), followed by the dropwise addition of a solution of 1-bromo-4-chloro-3,5-dimethoxybenzene (160 mg) in dry THF (2 mL). After the mixture was stirred for 20 minutes in the dry ice-methanol bath, triisopropyl borate (0.18 mL) was added and the mixture was additionally stirred for 20 minutes. The reaction mixture was then stirred at room temperature for 1 hour and pH of the mixture was adjusted at 3 using 4 M hydrochloric acid. The mixture was stirred at 0° C. for 1 hour and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and evaporated. The residue was recrystallized from ethyl acetate-hexane giving the title compound as white powder.

Yield: 90 mg (66%).

PREPARATION EXAMPLE 30 Synthesis of Ethyl 2-(4-Chloro-3,5-dimethoxyphenyl)isonicotinate

4-Chloro-3,5-dimethoxyphenylboronic acid (7.45 g) and ethyl 2-chloroisonicotinate (6.39 g) were condensedn in the same manner as described in Preparation Example 1 to give the title compound.

Yield: 8.55 g (77%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (t, 3H, J=7.3 Hz), 4.03 (s, 6H), 4.45 (q, 2H, J=7.3 Hz), 7.32 (s, 2H), 7.80 (d, 1H, J=5.1 Hz), 8.27 (s, 1H), 8.83 (d, 1H, J=5.0 Hz).

PREPARATION EXAMPLE 31 Synthesis of 2-(4-Chloro-3,5-dimethoxyphenyl)isonicotinic Acid

To a solution of ethyl 2-(4-chloro-3,5-dimethoxyphenyl)isonicotinate (8.55 g) in ethanol (80 mL) was added 2 M sodium hydroxide (100 mL). The mixture was refluxed for 30 min and evaporated. The aqueous layer was neutralized by 1 M hydrochloric acid and precipitates were dissolved in a mixed solvent of ethyl acetate-THF (3:1). After drying over anhydrous sodium sulfate, the solvent was evaporated to give the title compound.

Yield: 7.20 g (92%). ¹H-NMR (400 MHz, CDCl₃) δ: 4.02 (s, 6H), 7.34 (s, 2H), 7.83 (d, 1H, J=4.9 Hz), 7.84 (s, 1H), 8.82 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 32 Synthesis of 2-(4-Chloro-3,5-dimethoxyphenyl)-4-hydroxymethylpyridine

To an ice-cooled solution of 2-(4-chloro-3,5-dimethoxyphenyl)isonicotinic acid (7.20 g) and triethylamine (5.6 mL) in THF (70 mL) was added ethyl chloroformate (2.8 mL). The mixture was stirred at room temperature for 1 hour and filtered. To the filtrate was then added a solution of sodium borohydride (1.25 g) in water (4 mL). The mixture was stirred at room temperature for another hour and evaporated. Water was added to the residue and extracted with chloroform. The organic layer was washed with brine, dried over anhydrous sodium sulfate and evaporated. The residue was subjected to silica gel column chromatography using chloroform-methanol (20:1) and then chloroform-methanol (15:1) to give the title compound.

Yield: 4.10 g (60%). ¹H-NMR (400 MHz, CDCl₃+DMSO-d₆) δ: 4.01 (s, 6H), 4.76 (s, 2H), 7.20-7.35 (m, 3H), 7.78 (s, 1H), 8.62 (s, 1H).

PREPARATION EXAMPLE 33 Synthesis of 2-(4-Chloro-3,5-dimethoxyphenyl)-4-chloromethylpyridine

2-(4-Chloro-3,5-dimethoxyphenyl)-4-hydroxymethylpyridine (4.10 g) was treated in the same manner as described in Preparation Example 3 to give the title compound.

Yield: 4.20 g (96%). ¹H-NMR (400 MHz, CDCl₃) δ: 4.02 (s, 6H), 4.63 (s, 2H), 7.26 (s, 2H), 7.29 (d, 1H, J=4.9 Hz), 7.72 (s, 1H), 8.69 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 34 Synthesis of 1-[[2-(4-Chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]piperidine-4-carboxamide

Piperidine-4-carboxamide (301 mg) and 2-(4-chloro-3,5-dimethoxyphenyl) 4-chloromethyl pyridine (600 mg) were coupled in the same manner as described in Example 2 to give the title compound.

Yield: 743 mg (95%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.75-1.90 (m, 4H), 2.07-2.25 (m, 3H), 2.94 (d, 2H, J=11.6 Hz), 3.57 (s, 2H), 4.02 (s, 6H), 7.24-7.31 (m, 3H), 7.67 (s, 1H), 8.61 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 35 Synthesis of 1-[[2-(4-Chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]-4-(ethoxycarbonylamino)piperidine

1-[[2-(4-chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]piperidine-4-carboxamide (743 mg) was treated in the same manner as described in Preparation Example 20 to give the title compound.

Yield: 887 mg (theoretical amount). ¹H-NMR (400 MHz, CDCl₃) δ: 1.24 (t, 3H, J=7.1 Hz), 1.43-1.59 (m, 2H), 1.96 (d, 2H, J=11.4 Hz), 2.19 (t, 2H, J=11.0 Hz), 2.82 (d, 2H, J=11.5 Hz), 3.56 (s, 2H), 4.02 (s, 6H), 4.10 (q, 2H, J=7.1 Hz), 7.26 (s, 2H), 7.66 (s, 1H), 7.71 (dd, 1H, J=5.6 Hz, 1.0 Hz), 8.6 (dd, 1H, J=4.9 Hz, 0.5 Hz).

PREPARATION EXAMPLE 36 Synthesis of 1-[[2-(4-Chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]-4-methylaminopiperidine

1-[[2-(4-chloro-3,5-diemthoxyphenyl)pyridin-4-yl]methyl]-4-(ethoxy-carbonylamino)piperidine (887 mg) was treated in the same manner as described in Preparation Example 21 to give the title compound.

Yield: 195 mg (27%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.35-1.49 (m, 2H), 1.89 (d, 2H, J=12.3 Hz), 2.11 (t, 2H, J=9.4 Hz), 2.38-2.45 (m, 1H), 2.44 (s, 3H), 2.87 (d, 2H, J=10.7 Hz), 3.57 (s, 2H), 4.02 (s, 6H), 7.23-7.29 (m, 3H), 7.68 (s, 1H), 8.61 (d, 1H, J=4.9 Hz).

EXAMPLE 8

 

Synthesis of 1-[[2-(4-Chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[[2-(4-chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]-N-methylamino]piperidine Tetrahydrochloride

1-[[2-(4-chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]-4-methylamino-piperidine (195 mg) and 2-(4-chloro-3,5-dimethoxyphenyl)-4-chloromethylpyridine (152 mg) were condensed in the same manner as described in Example 2. A free base obtained was converted to a tetrahydrochloride giving yellow powder.

Yield: 300 mg (75%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.60-1.90 (m, 4H), 2.06 (t, 2H, J=11.7 Hz), 2.26 (s, 3H), 2.45-2.55 (m, 1H), 2.97 (d, 2H, J=11.3 Hz), 3.57 (s, 2H), 3.67 (s, 2H), 4.01 (s, 6H), 4.02 (s, 6H), 7.24-7.28 (m, 6H), 7.65 (s, 1H), 7.67 (s, 1H), 8.61 (d, 1H, J=5.4 Hz), 8.62 (d, 1H, J=5.4 Hz).

PREPARATION EXAMPLE 37 Synthesis of 4-(p-Anisidino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-piperidine

To a solution of 1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone (2.17 g) in toluene (40 mL) was added p-anisidine (900 mg) and molecular sieves 4A (6.0 g). The mixture was refluxed overnight, then filtered and the filtrate was evaporated. The residual oil was dissolved in ethanol (40 mL) and sodium borohydride (276 mg) was added. The mixture was stirred at room temperature for 2 hours before concentration in vacuo. The residue was dissolved in ethyl acetate, washed with brine, dried over anhydrous sodium sulfate and evaporated. The residual oil was subjected to silica gel column chromatography using chloroform-methanol (50:1) to give the title compound as yellow amorphous.

Yield: 1.56 g (55%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.48 (br, 2H), 2.05 (br, 2H), 2.20 (br, 2H), 2.86 (br, 2H), 3.23 (s, 1H), 3.58 (s, 2H), 3.74 (s, 3H), 3.91 (s, 3H), 3.97 (s, 6H), 6.58 (d, 2H, J=8.8 Hz), 6.77 (d, 2H, J=9.0 Hz), 7.22 (d, 1H, J=5.1 Hz), 7.26 (s, 2H), 7.64 (s, 1H), 8.59 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 38 Synthesis of Ethyl 2-(3,4,5-Trimethoxyphenyl)nicotinate

3,4,5-Trimethoxyphenylboronic acid (694 mg) and ethyl 2-chloronicotinate (608 mg) were reacted in the same manner as described in Preparation Example 1 to give the title compound.

Yield: 799 mg (77%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.10 (t, 3H, J=7.2 Hz), 3.89 (s, 9H), 4.19 (q, 2H, J=7.2 Hz), 6.79 (s, 2H), 7.34 (dd, 1H, J=7.8 Hz, 4.8 Hz), 8.06 (dd, 1H, J=7.8 Hz, 1.7 Hz), 8.75 (dd, 1H, J=4.8 Hz, 1.7 Hz).

PREPARATION EXAMPLE 39 Synthesis of 3-Hydroxymethyl-2-(3,4,5-trimethoxyphenyl)pyridine

Ethyl 2-(3,4,5-trimethoxyphenyl)nicotinate (468 mg) was treated in the same manner as described in Preparation Example 2 to give the title compound.

Yield: 293 mg (72%). ¹H-NMR (400 MHz, CDCl₃) δ: 3.90 (s, 9H), 4.72 (s, 2H), 6.83 (s, 2H), 7.32 (dd, 1H, J=7.9 Hz, 4.8 Hz), 7.92 (dd, 1H, J=7.9 Hz, 1.7 Hz), 8.62 (dd, 1H, J=4.8 Hz, 1.7 Hz).

PREPARATION EXAMPLE 40 Synthesis of 3-Chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine

3-Hydroxymethyl-2-(3,4,5-trimethoxyphenyl)pyridine (293 mg) was treated in the same manner as described in the Preparation Example 3 to give the title compound.

Yield: 311 mg (theoretical amount).

EXAMPLE 9

 

Synthesis of 4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-3-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

To a solution of 4-(p-anisidino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (139 mg) and 3-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) in acetonitrile (5 ml) was added potassium carbonate (83 mg) and potassium iodide (63 mg). The mixture was stirred at 70° C. overnight and evaporated. The residue was dissolved in chloroform, washed with water and brine, dried over anhydrous magnesium sulfate and evaporated. The residual oil was applied to a column of silica gel using diethylether-metanol (20:1) as an eluent. A free base obtained was converted to a trihydrochloride to give the title compound as yellow powder.

Yield: 16 mg, (8%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.60 (br, 2H), 1.77 (br, 2H), 2.09 (br, 2H), 2.93 (br, 2H), 3.45 (br, 1H), 3.54 (s, 2H), 3.73 (s, 3H), 3.90 (s, 6H), 3.91 (s, 6H), 3.96 (s, 6H), 4.34 (s, 2H), 6.65 (d, 2H, J=9.0 Hz), 6.71 (s, 2H), 6.74 (d, 2H, J=9.0 Hz), 7.16-7.19 (m, 2H), 7.22 (s, 2H), 7.55 (s, 1H), 7.79 (d, 1H, J=7.0 Hz), 8.50 (br, 1H), 8.58 (d, 1H, J=4.9 Hz).

EXAMPLE 10

 

Synthesis of 4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxypheny)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(p-Anisidino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (1.56 g) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (1.08 g) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a trihydrochloride which gave the title compound as yellow powder.

Yield: 1.17 g (40%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.68-1.97 (m, 4H), 2.09-2.23 (m, 2H), 2.98 (br, 2H), 3.54-3.66 (m, 3H), 3.73 (s, 3H), 3.89 (s, 3H), 3.90 (s, 3H), 3.93 (s, 6H), 3.96 (s, 6H), 4.45 (s, 2H), 6.74 (d, 2H, J=9.2 Hz), 6.79 (d, 2H, J=9.2 Hz), 7.15 (s, 2H), 7.16-7.21 (m, 2H), 7.23 (s, 2H), 7.57 (s, 1H), 7.60 (s, 1H), 8.54 (d, 1H, J=5.1 Hz), 8.59 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 41 Synthesis of 3-(3,4,5-Trimethoxyphenyl)benzyl Alcohol

Ethyl 3-(3,4,5-trimethoxyphenyl)benzoate (5.09 g) was treated in the same manner as described in Preparation Example 2 to give the title compound.

Yield: 4.25 g (97%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.87 (t, 1H, J=6.0 Hz), 3.89 (s, 3H), 3.92 (s, 6H), 4.76 (d, 1H, J=5.6 Hz), 6.77 (s, 2H), 7.34 (d, 1H, J=7.4 Hz), 7.42 (t, 1H, J=7.5 Hz), 7.48 (d, 1H, J=7.6 Hz), 7.55 (s, 1H).

PREPARATION EXAMPLE 42 Synthesis of 3-(3,4,5-Trimethoxyphenyl)benzyl Chloride

3-(3,4,5-Trimethoxyphenyl)benzyl alcohol (1.21 g) was treated in the same manner as described in Preparation Example 3 to give the title compound.

Yield: 893 mg (69%). ¹H-NMR (400 MHz, CDCl₃) δ: 3.87 (s, 3H), 3.90 (s, 6H), 4.62 (s, 2H), 6.75 (s, 2H), 7.33 (d, 1H, J=7.6 Hz), 7.39 (t, 1H, J=7.7 Hz), 7.48 (d, 1H, J=7.6 Hz), 7.54 (s, 1H).

EXAMPLE 11

 

Synthesis of 4-[N-(4-Methoxyphenyl)-N-[3-(3,4,5-trimethoxypheny)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

4-(p-Anisidino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (139 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a dihydrochloride which gave the title compound as yellow powder.

Yield: 52 mg (22%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.77-1.92 (m, 5H), 2.14-2.20 (m, 2H), 2.95-3.00 (m, 5H), 2.14-2.20 (m, 2H), 2.95-3.00 (m, 2H), 3.58 (s, 2H), 3.72 (s, 3H), 3.88 (s, 3H), 3.89 (s, 6H), 3.90 (s, 3H), 3.96 (s, 6H), 4.47 (s, 2H), 6.70 (s, 2H), 6.74-6.83 (m, 4H), 7.20 (d, 1H, J=7.4 Hz), 7.23 (s, 2H), 7.25-7.27 (m, 1H), 7.33 (t, 1H, J=7.4 Hz), 7.38 (d, 1H, J=8.7 Hz), 7.43 (s, 1H), 7.62 (s, 1H), 8.59 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 43 Synthesis of Ethyl 6-(3,4,5-Trimethoxyphenyl)nicotinate

3,4,5-Trimethoxyphneylboronic acid (1.16 g) and ethyl 6-chloronitotinate (1.02 g) were coupled in the same manner as described in the Preparation Example 1 to give the title compound.

Yield: 1.42 g (82%) ¹H-NMR (400 MHz, CDCl₃) δ: 1.43 (t, 3H, J=7.2 Hz), 3.92 (s, 3H), 3.98 (s, 6H), 4.44 (q, 2H, J=7.2 Hz), 7.32 (s, 2H), 7.76 (d, 1H, J=8.3 Hz), 8.33 (dd, 1H, J=8.2 Hz, 2.2 Hz), 9.26 (d, 1H, J=2.2 Hz).

PREPARATION EXAMPLE 44 Synthesis of 5-Hydroxymethyl-2-(3,4,5-trimethoxyphenyl)pyridine

Ethyl 6-(3,4,5-trimethoxyphenyl)nicotinate (658 mg) was treated in the same manner as described in Preparation Example 2 to give the title compound.

Yield: 482 mg (85%). ¹H-NMR (400 MHz, CDCl₃) δ: 3.91 (s, 3H), 3.97 (s, 6H), 4.76 (s, 2H), 7.23 (s, 2H), 7.68 (d, 1H, J=7.4 Hz), 7.78 (dd, 1H, J=7.4 Hz, 2.3 Hz), 8.63 (d, 1H, J=2.3 Hz).

PREPARATION EXAMPLE 45 Synthesis of 5-Chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine

5-Hydroxymethyl-2-(3,4,5-trimethoxyphenyl)pyridine (685 mg) was treated in the same manner as described in Preparation Example 3 to give the title compound.

Yield: 717 mg (theoretical amount).

EXAMPLE 12

 

Synthesis of 4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(p-Anisidino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (139 mg) and 5-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a trihydrochloride which gave the title compound as yellow powder.

Yield: 13 mg (5%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.76 (br, 2H), 1.88 (br, 2H), 2.14 (br, 2H), 2.97 (br, 2H), 3.51 (br, 1H), 3.57 (s, 2H), 3.73 (s, 3H), 3.89 (s, 3H), 3.90 (s, 3H), 3.94 (s, 6H), 3.96 (s, 6H), 4.42 (s, 2H), 6.78 (br, 4H), 7.20 (br, 3H), 7.23 (s, 2H), 7.57-7.70 (m, 3H), 8.58-8.60 (m, 2H).

PREPARATION EXAMPLE 46 Synthesis of Ethyl 5-(3,4,5-Trimethoxyphenyl)nicotinate

3,4,5-Trimethoxyphenylboronic acid (6.36 g) and ethyl 5-bromonicotinate (6.90 g) were reacted in the same manner as described in Preparation Example 1 to give the title compound.

Yield: 7.19 g (76%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.44 (t, 3H, J=7.1 Hz), 3.91 (s, 3H), 3.95 (s, 6H), 4.46 (q, 2H, J=7.1 Hz), 6.79 (s, 2H), 8.44 (t, 1H, J=2.1 Hz), 8.96 (d, 1H, J=2.1 Hz), 9.18 (d, 1H, J=1.8 Hz).

PREPARATION EXAMPLE 47 Synthesis of 3-Hydroxymethyl-5-(3,4,5-trimethoxyphenyl)pyridine

Ethyl 5-(3,4,5-trimethoxyphenyl)nicotinate (7.19 g) was treated in the same manner as described in the Preparation Example 2 to give the title compound.

Yield; 3.83 g (61%). ¹H-NMR (400 MHz, CDCl₃) δ: 3.88 (s, 3H), 3.89 (s, 6H), 4.39 (br, 1H), 4.80 (s, 2H), 6.72 (s, 2H), 7.89 (t, 1H, J=1.2 Hz), 8.47 (d, 1H, J=2.1 Hz), 8.63 (d, 1H, J=2.2 Hz).

PREPARATION EXAMPLE 48 Synthesis of 3-Chloromethyl-5-(3,4,5-trimethoxyphenyl)pyridine

3-Hydroxymethyl-5-(3,4,5-trimethoxyphenyl)pyridine (2.85 g) was treated in the same manner as described in Preparation Example 3 to give the title compound.

Yield: 1.97 g (65%). ¹H-NMR (400 MHz, CDCl₃) δ: 3.90 (s, 3H), 3.94 (s, 6H), 4.67 (s, 2H), 6.75 (s, 2H), 7.87 (t, 1H, J=2.1 Hz), 8.59 (d, 1H, J=2.0 Hz), 8.76 (d, 1H, J=2.1 Hz).

EXAMPLE 13

 

Synthesis of 4-[N-(4-Methoxyphenyl)-N-[[5-(3,4,5-trimethoxyphenyl)pyridin-3-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(p-Anisidino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (139 mg) and 3-chloromethyl-5-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a trihydrochloride which gave the title compound as yellow powder.

Yield: 14 mg (5%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ; 1.73-1.75 (m, 2H), 1.88 (d, 2H, J=11.3 Hz), 2.13 (t, 2H, J=11.3 Hz), 2.96 (d, 2H, J=11.5 Hz), 3.50 (br, 1H), 3.55 (s, 2H), 3.72 (s, 3H), 3.88 (s, 3H), 3.89 (s, 9H), 3.96 (s, 6H), 4.45 (s, 2H), 6.65 (s, 2H), 6.76 (d, 2H, J=9.6 Hz), 6.80 (d, 2H, J=9.4 Hz), 7.20 (d, 1H, J=5.3 Hz), 7.22 (s, 2H), 7.59 (s, 1H), 7.67 (s, 1H), 8.50 (s, 1H), 8.59 (d, 1H, J=4.7 Hz), 8.62 (s, 1H).

PREPARATION EXAMPLE 49 Synthesis of 2,6-Dimethoxy-4-iodophenol

To a solution of 5-iodo-1,2,3-trimethoxybenzene (3.2 g) in 1,2-dichloroethane (40 mL) was added aluminum chloride (1.6 g). The mixture was stirred at 60° C. for 4 hours and evaporated. The residue was dissolved in 1 M aqueous sodium hydroxide solution and washed with ether. The aqueous layer was then acidified and extracted with chloroform. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and evaporated to give the title compound as white crystalline powder.

Yield: 1.0 g (31%)

PREPARATION EXAMPLE 50 Synthesis of 1,3-Dimethoxy-5-iodo-2-isopropoxybenzene

To a suspension of 2,6-dimethoxy-4-iodophenol (1.0 g) and potassium carbonate (938 mg) in DMF (10 mL) was added isopropyl iodide (507 □L). The mixture was stirred at 60° C. for 3 hours and evaporated. Ethyl acetate and water were added to the residue, the organic layer was separated, washed with brine, dried over anhydrous sodium sulfate and evaporated. The residue was applied to a column of silica gel using hexane-ethyl acetate (5:1) as an eluent to give the title compound.

Yield: 788 mg (72%).

PREPARATION EXAMPLE 51 Synthesis of 3,5-Dimethoxy-4-isopropoxyphenylboronic Acid

1,3-Dimethoxy-5-iodo-2-isopropoxybenzene (2.25 g) was treated in the same manner as described in Preparation Example 27 to give the title compound.

Yield: 1.23 g (74%).

PREPARATION EXAMPLE 52 Synthesis of Ethyl 2-(3,5-Dimethoxy-4-isopropoxyphenyl)isonicotinate

To a solution of 3,5-dimethoxy-4-isopropoxyphenylboronic acid (1.23 g) and ethyl 2-chloroisonicotinate (0.95 g) were condensed in the same manner as described in Preparation Example 1 to give the title compound.

Yield: 1.57 g(89%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.33 (d, 6H, J=4.9 Hz), 1.44 (t, 3H, J=7.1 Hz), 3.95 (s, 6H), 4.42-4.49 (m, 3H), 7.29 (s, 2H), 7.75 (dd, 1H, J=4.9 Hz, 1.4 Hz), 8.24 (s, 1H), 8.80 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 53 Synthesis of 2-(3,5-Dimethoxy-4-isopropoxyphenyl)-4-hydroxymethylpyridine

Ethyl 2-(3,5-dimethoxy-4-isopropoxyphenyl)isonicotinate (1.57 g) was treated in the same manner as described in the Preparation Example 2 to give the title compound.

Yield: 1.27 g (92%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.32 (d, 6H, J=6.1 Hz), 3.93 (s, 6H), 4.45 (quint, 1H, J=6.1 Hz), 4.81 (s, 2H), 7.20 (d, 1H, J=5.1 Hz), 7.23 (s, 2H), 7.68 (s, 1H), 8.62 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 54 Synthesis of 4-Chloromethyl-2-(3,5-dimethoxy-4-isopropoxyphenyl)pyridine

2-(3,5-Dimethoxy-4-isopropoxyphenyl)-4-hydroxymethylpyridine (1.49 g) was treated in the same manner as described in Preparation Example 3 to give the title compound.

Yield: 1.33 g (84%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.32 (d, 6H, J=6.2 Hz), 3.94 (s, 6H), 4.45 (quint, 1H, J=6.1 Hz), 4.61 (s, 2H), 7.23-7.26 (m, 3H), 7.69 (s, 1H), 8.66 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 55 Synthesis of 1-[[2-(3,5-Dimethoxy-4-isopropoxyphenyl)pyridin-4-yl]methyl]-4-piperidone Ethylene Ketal

4-Chloromethyl-2-(3,5-dimethoxy-4-isopropoxyphenyl)pyridine (643 mg) and 4-piperidone ethylene ketal (287 mg) were coupled in the same manner as described in Example 2 to give the title compound.

Yield: 818 mg (95%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.32 (d, 6H, J=6.1 Hz), 1.78 (t, 4H, J=5.7 Hz), 2.57 (br, 4H), 3.49 (s, 4H), 3.59 (s, 2H), 3.94 (s, 6H), 4.44 (quint, 1H, J=6.1 Hz), 7.21 (d, 1H, J=5.1 Hz), 7.23 (s, 2H), 7.65 (s, 1H), 8.59 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 56 Synthesis of 1-[[2-(3,5-Dimethoxy-4-isopropoxyphenyl)pyridin-4-yl]methyl]-4-piperidone

1-[[2-(3,5-Dimethoxy-4-isopropoxyphenyl)pyridin-4-yl]methyl]-4-piperidone ethylene ketal (818 mg) was treated in the same manner as described in Preparation Example 23 to give the title compound.

Yield: 717 mg (98%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.32 (d, 6H, J=6.2 Hz), 2.50 (t, 4H, J=6.1 Hz), 2.81 (t, 4H, J=6.1 Hz), 3.69 (s, 2H), 3.95 (s, 6H), 4.45 (quint, 1H, J=6.2 Hz), 7.24 (s, 2H), 7.25-7.27 (m, 1H), 7.68 (s, 1H), 8.63 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 57 Synthesis of 4-(p-Anisidino)-1-[[2-(3,5-dimethoxy-4-isopropoxyphenyl)pyridin-4-yl]methyl]piperidine

1-[[2-(3,5-dimethoxy-4-isopropoxyphenyl)pyridin-4-yl]methyl]-4-piperidone (350 mg) and p-anisidine (123 mg) were condensed in the same manner as described in Preparation Example 37 to give the title compound.

Yield: 307 mg (69%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.32 (d, 6H, J=6.3 Hz), 1.46-1.52 (m, 2H), 2.00-2.24 (m, 2H), 2.22 (t, 2H, J=11.1 Hz), 2.86 (d, 2H, J=12.1 Hz), 3.18-3.28 (m, 1H), 3.58 (s, 2H), 3.74 (s, 3H), 3.94 (s, 6H), 4.40 (quint, 1H, J=6.3 Hz), 6.58 (d, 2H, J=6.6 Hz), 6.78 (d, 2H, J=6.6 Hz), 7.20 (d, 1H, J=5.1 Hz), 7.24 (s, 2H), 7.64 (s, 1H), 8.59 (d, 1H, J=5.1 Hz).

EXAMPLE 14

 

Synthesis of 1-[[2-(3,5-Dimethoxy-4-isopropoxyphenyl)pyridin-4-yl]methyl]-4-[N-[[2-(3,5-dimethoxy-4-isopropoxyphenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine Trihydrochloride

4-(p-anisidino)-1-[[2-(3,5-dimethoxy-4-isopropoxyphenyl)pyridin-4-yl]methyl]piperidine (307 mg) and 4-chloromethyl-2-(3,5-dimethoxy-4-isopropoxyphenyl)pyridine (201 mg) were condensed in the same manner as described in Example 9. A free base obtained was converted to a trihydrochloride giving the title compound as yellow powder.

Yield: 230 mg (46%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.31 (d, 6H, J=3.3 Hz), 1.32 (d, 6H, J=6.8 Hz), 1.70-1.92 (m, 4H), 2.10-2.20 (m, 2H), 2.92-3.01 (m, 2H), 3.56 (s, 2H), 3.73 (s, 3H), 3.85-3.95 (m, 1H), 3.90 (s, 6H), 3.93 (s, 6H), 4.39-4.49 (m, 4H), 6.73 (d, 2H, J=4.8 Hz), 6.78 (d, 2H, J=4.8 Hz), 7.14 (s, 2H), 7.15-7.20 (m, 2H), 7.23 (s, 2H), 7.58 (s, 1H), 7.60 (s, 1H), 8.53 (d, 1H, J=5.1 Hz), 8.58 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 58 Synthesis of 4-Benzylamino-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]-methyl]piperidine

1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl-4-piperidone (1.40 g) and benzylamine (0.51 g) was condensed in the same manner as described in Preparation Example 37 to give the title compound as yellow amorphous.

Yield: 1.20 g (68%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.40-1.60 (m, 2H), 1.88-2.09 (m, 5H), 2.54 (br, 1H), 2.82-2.85 (m, 2H), 3.52 (s, 2H), 3.80 (s, 2H), 3.89 (s, 2H), 3.95 (s, 6H), 7.18-7.31 (m, 8H), 7.64 (s, 1H), 8.57 (d, 1H, J=5.1 Hz).

EXAMPLE 15

 

Synthesis of 4-[N-Benzyl-N-[[2-(3,4,5-trimethoxypheny)pyridin-3-yl]-methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Tetrahydrochloride

4-Benzylamino-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (134 mg) and 3-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed in the same manner as described in Example 9. A free base obtained was converted to a tetrahydrochloride to give the title compound as yellow powder.

Yield: 43 mg, (17%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.63 (br, 4H), 1.87 (br, 2H), 2.39 (br, 1H), 2.88 (br, 2H), 3.49 (s, 2H), 3.57 (s, 2H), 3.68 (s, 2H), 3.86 (s, 6H), 3.88 (s, 3H), 3.90 (s, 3H), 3.96 (s, 6H), 6.60 (s, 2H), 7.17 (d, 1H, J=5.1 Hz), 7.22-7.29 (m, 8H), 7.56 (s, 1H), 8.02 (d, 1H, J=8.0 Hz), 8.50 (d, 1H, J=6.4 Hz), 8.58 (d, 1H, J=5.1 Hz).

EXAMPLE 16

 

Synthesis of 4-[N-Benzyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Tetrahydrochloride

4-Benzylamino-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (230 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (158 mg) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a tetrahydrochloride which gave the title compound as yellow powder.

Yield: 172 mg (47%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.69-1.85 (m, 4H), 1.93-1.99 (m, 2H), 2.56 (br, 1H), 2.93-3.00 (m, 2H), 3.51 (s, 2H), 3.71 (s, 2H), 3.74 (s, 2H), 3.90 (s, 6H), 3.96 (s, 6H), 3.96 (s, 6H), 7.18-7.32 (m, 9H), 7.38 (d, 2H, J=7.1 Hz), 7.59 (s, 1H), 7.68 (s, 1H), 8.56 (d, 1H, J=5.1 Hz), 8.60 (d, 1H, J=5.1 Hz).

EXAMPLE 17

 

Synthesis of 4-[N-Benzyl-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-Benzylamino-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (134 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a trihydrochloride which gave the title compound as yellow powder.

Yield: 47 mg (18%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.70-1.86 (m, 4H), 1.96 (br, 2H), 2.59 (br, 1H), 2.94 (br, 2H), 3.51 (s, 2H), 3.70 (s, 2H), 3.74 (s, 2H), 3.89 (s, 3H), 3.90 (s, 3H), 3.92 (s, 6H), 3.96 (s, 6H), 6.75 (s, 2H), 7.18-7.30 (m, 6H), 7.35-7.40 (m, 5H), 7.56 (s, 1H), 7.60 (s, 1H), 8.58 (d, 1H, J=5.1 Hz).

EXAMPLE 18

 

Synthesis of 4-[N-Benzyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Tetrahydrochloride

4-Benzylamino-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (134 mg) and 5-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a tetrahydrochloride which gave the title compound as yellow powder.

Yield: 44 mg (17%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.81 (br, 4H), 1.96 (br, 2H), 2.55 (br, 1H), 2.96 (br, 2H), 3.52 (s, 2H), 3.69 (s, 4H), 3.89 (s, 6H), 3.95 (s, 6H), 3.96 (s, 6H), 7.19-7.32 (m, 8H), 7.36-7.38 (m, 2H), 7.61 (d, 2H, J=7.6 Hz), 7.69-7.73 (m, 1H), 8.59 (d, 1H, J=4.9 Hz), 8.63 (s, 1H).

EXAMPLE 19

 

Synthesis of 4-[N-Benzyl-N-[[5-(3,4,5-trimethoxypheny)pyridin-3-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Tetrahydrochloride

4-Benzylamino-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (134 mg) and 3-chloromethyl-5-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a tetrahydrochloride which gave the title compound as yellow powder.

Yield: 26 mg (10%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.83 (br, 4H), 1.97 (br, 2H), 2.58 (br, 1H), 2.95 (br, 2H), 3.53 (s, 2H), 3.71 (s, 2H), 3.75 (s, 2H), 3.90 (s, 6H), 3.93 (s, 6H), 3.96 (s, 6H), 6.74 (s, 2H), 7.19-7.30 (m, 6H), 7.36 (d, 2H, J=6.8 Hz), 7.60 (s, 1H), 7.79 (s, 1H), 8.54 (s, 1H), 8.59 (d, 1H, J=5.1 Hz), 8.64 (s, 1H).

PREPARATION EXAMPLE 59 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[[2-(3,4,5-trmethoxyphenyl)pyridin-4-yl]methyl]aminomethyl]piperidine

1-(tert-Butoxycarbonyl)-4-aminomethylpiperidine (200 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (183 mg) were condensed in the same manner as described in Example 2 to give the title compound as yellow syrup.

Yield: 264 mg (90%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.12-1.27 (m, 3H), 1.45 (s, 9H), 1.60 (br, 1H), 1.74 (d, 2H, J=12.9 Hz), 2.54 (d, 2H, J=6.6 Hz), 2.69 (br, 2H), 3.87 (s, 2H), 3.90 (s, 3H), 3.97 (s, 6H), 4.03-4.14 (m, 2H), 7.20 (d, 1H, J=3.9 Hz), 7.24 (s, 2H), 7.65 (s, 1H), 8.60 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 60 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-methyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]aminomethyl]piperidine

1-(tert-butoxycarbonyl)-4-[N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]aminomethyl]piperidine (264 mg) was treated in the same manner as described in Preparation Example 11 to give the title compound as yellow syrup.

Yield: 157 mg (58%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.00-1.09 (m, 2H), 1.43 (s, 9H), 1.65-1.70 (m, 1H), 1.79 (d, 2H, J=12.7 Hz), 2.21 (d, 2H, J=7.4 Hz), 2.23 (s, 3H), 2.69 (br, 2H), 3.52 (s, 2H), 3.89 (s, 3H), 3.96 (s, 6H), 4.07-4.13 (m, 2H), 7.20 (d, 1H, J=4.9 Hz), 7.24 (s, 2H), 7.64 (s, 1H), 8.58 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 61 Synthesis of 4-[N-Methyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]aminomethyl]piperidine

1-(tert-Butoxycarbonyl)-4-[N-methyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]aminomethyl]piperidine (152 mg) was treated in the same manner as described in Preparation Example 12 to give the title compound as yellow crystals.

Yield: 105 mg (88%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.00-1.10 (m, 2H), 1.60-1.68 (m, 1H), 1.80 (d, 2H, J=12.5 Hz), 2.03 (br, 1H), 2.20 (d, 2H, J=8.4 Hz), 2.21 (s, 3H), 2.58 (dt, 2H, J=12.1 Hz, 2.1 Hz), 3.05 (d, 2H, J=12.1 Hz), 3.51 (s, 2H), 3.89 (s, 3H), 3.95 (s, 6H), 7.20 (d, 1H, J=5.1 Hz), 7.24 (s, 2H), 7.65 (s, 1H), 8.57 (d, 1H, J=5.9 Hz).

EXAMPLE 20

 

Synthesis of 4-[N-Methyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]aminomethyl]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dioxalate

4-[N-methyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino-methyl]piperidine (96 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (73 mg) were condensed in the same manner as described in Example 2. The title compound was obtained as white powder after converting a free base to a dioxalate.

Yield: 109 mg (40%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.19-1.2? (m, 2H), 1.56 (br, 1H), 1.81 (d, 2H, J=11.1 Hz), 1.99-2.04 (m, 2H), 2.23 (s, 5H), 2.88 (d, 2H, J=11.1Hz), 3.53 (s, 4H), 3.89 (s, 3H), 3.90 (s, 3H), 3.94 (s, 6H), 3.96 (s, 6H), 7.20 (br, 2H), 7.23 (s, 4H), 7.61 (s, 1H), 7.64 (s, 1H), 8.58 (d, 2H, J=4.9 Hz).

PREPARATION EXAMPLE 62 Synthesis of 4-(3,5-Dimethoxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine

1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl-4-piperidone (1.40 g) and 3,5-dimethoxyaniline (722 mg) were treated in the same manner as described in Preparation Example 37 to give the title compound.

Yield: 800 mg (41%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.40-1.90 (m, 2H), 1.95-2.50 (m, 4H), 2.93 (br, 2H), 3.31 (br, 1H), 3.65 (br, 2H), 3.72 (s, 6H), 3.88 (s, 3H), 3.96 (s, 6H), 5.76 (s, 2H), 5.85 (s, 1H), 7.20-7.35 (m, 3H), 7.73 (br, 1H), 8.60 (d, 1H, J=4.9 Hz).

EXAMPLE 21

 

Synthesis of 4-[N-(3,5-Dimethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-3-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(3,5-Dimethoxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (148 mg) and 3-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed in the same manner as described in Example 9. Yellow syrup obtained was converted to a trihydrochloroide to give the title compound as yellow powder.

Yield: 29 mg, (11%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.60-1.63 (m, 2H), 1.79 (d, 2H, J=11.7 Hz), 2.13 (t, 2H, J=11.4 Hz), 2.94 (d, 2H, J=11.3 Hz), 3.54 (s, 2H), 3.71 (s, 6H), 3.78-3.84 (m, 1H), 3.90 (s, 3H), 3.91 (s, 6H), 3.92 (s, 3H), 3.96 (s, 6H), 4.41 (s, 2H), 5.84 (s, 2H), 6.72 (s, 2H), 7.09-7.24 (m, 5H), 7.53 (s, 1H), 7.71 (d, 1H, J=6.6 Hz), 8.51 (dd, 1H, J=4.7 Hz, 1.6 Hz), 8.59 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 63 Synthesis of Ethyl 2-(3,4,5-Trimethoxyphenyl)benzoate

3,4,5-Trimethoxyphenylboronic acid (639 mg) and ethyl 2-bromobenzoate (479 mg) were condensed in the same manner as described in Preparation Example 1 to give the title compound.

Yield: 655 mg (69%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.04 (t, 3H, J=7.2 Hz), 3.86 (s, 6H), 3.89 (s, 3H), 4.12 (q, 2H, J=7.2 Hz), 6.54 (s, 2H), 7.40-7.42 (m, 2H), 7.51 (t, 1H, J=7.8 Hz), 7.77 (d, 1H, J=6.8 Hz).

PREPARATION EXAMPLE 64 Synthesis of 2-(3,4,5-Trimethoxyphenyl)benzyl Alcohol

Ethyl 2-(3,4,5-trimethoxyphenyl)benzoate (655 mg) was treated in the same manner as described in Preparation Example 2 to give the title compound.

Yield: 630 mg (theoretical amount). ¹H-NMR (400 MHz, CDCl₃) δ: 3.85 (s, 6H), 3.90 (s, 3H), 4.61 (s, 2H), 6.61 (s, 2H), 7.26-7.39 (m, 3H), 7.53 (d, 1H, J=6.8 Hz).

PREPARATION EXAMPLE 65 Synthesis of 2-(3,4,5-Trimethoxyphneyl)benzyl Chloride

2-(3,4,5-Trimethoxyphenyl)benzyl alcohol (630 mg) was treated in the same manner as described in Preparation Example 3 to give the title compound.

Yield: 615 mg (theoretical amount). ¹H-NMR (400 MHz, CDCl₃) δ: 3.87 (s, 6H), 3.90 (s, 3H), 4.53 (s, 2H), 6.66 (s, 2H), 7.29-7.32 (m, 1H), 7.34-7.39 (m, 2H), 7.50-7.52 (m, 1H).

EXAMPLE 22

 

Synthesis of 4-[N-(3,5-Dimethoxyphenyl)-N-[2-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

4-(3,5-Dimethoxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (148 mg) and 2-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed in the same manner as described in Example 9. A free base obtained was converted to a dihydrochloroide to give the title compound as yellow powder.

Yield: 20 mg, (8%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.50-1.90 (m, 4H), 2.05-2.20 (m, 2H), 2.92 (br, 2H), 3.52 (br, 3H), 3.68 (s, 6H), 3.85 (s, 6H), 3.88 (s, 3H), 3.89 (s, 3H), 3.94 (s, 6H), 4.31 (s, 2H), 5.85 (br, 3H), 6.52 (s, 2H), 7.05-7.27 (m, 6H), 7.34 (s, 1H), 7.51 (s, 1H), 8.56 (s, 1H).

EXAMPLE 23

 

Synthesis of 4-[N-(3,5-Dimethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(3,5-Dimethoxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (148 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a trihydrochloride which gave the title compound as yellow powder.

Yield: 40 mg (18%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.68-1.90 (m, 4H), 2.12-2.22 (m, 2H), 2.94-3.02 (m, 2H), 3.57 (s, 2H), 3.71 (s, 6H), 3.81-3.83 (m, 1H), 3.89 (s, 3H), 3.90 (s, 3H), 3.93 (s, 6H), 3.96 (s, 6H), 4.52 (s, 2H), 5.89-5.94 (m, 3H), 7.14 (d, 1H, J=5.3 Hz), 7.16 (s, 2H), 7.20 (d, 1H, J=3.7 Hz), 7.22 (s, 2H), 7.54-7.60 (m, 2H), 8.55 (d, 1H, J=5.1 Hz), 8.59 (d, 1H, J=5.1 Hz).

EXAMPLE 24

 

Synthesis of 4-[N-(3,5-Dimethoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

4-(3,5-Dimethoxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (148 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a dihydrochloride which gave the title compound as yellow powder.

Yield: 41 mg (16%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.78-1.88 (m, 4H), 2.16 (t, 2H, J=10.7 Hz), 2.96 (d, 2H, J=11.3 Hz), 3.56 (s, 2H), 3.70 (s, 6H), 3.73-3.84 (m, 1H), 3.87 (s, 3H), 3.89 (s, 6H), 3.90 (s, 3H), 3.95 (s, 6H), 4.54 (s, 2H), 5.95 (s, 2H), 6.71 (s, 2H), 7.19-7.26 (m, 4H), 7.31-7.39 (m, 3H), 7.42 (s, 1H), 7.59 (s, 1H), 8.58 (d, 1H, J=4.9 Hz).

EXAMPLE 25

 

Synthesis of 4-[N-(3,5-Dimethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(3,5-Dimethoxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (148 mg) and 5-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a trihydrochloride which gave the title compound as yellow powder.

Yield: 23 mg (10%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.64 (br, 2H), 1.82 (br, 2H), 2.10 (br, 2H), 2.94 (br, 2H), 3.48-3.60 (m, 3H), 3.64 (s, 6H), 3.82 (s, 3H), 3.83 (s, 3H), 3.87 (s, 6H), 3.90 (s, 6H), 4.46 (s, 2H), 5.85 (br, 3H), 7.05-7.24 (m, 6H), 7.53-7.54 (m, 2H), 8.51 (s, 1H), 8.54 (br, 1H).

PREPARATION EXAMPLE 66 Synthesis of Ethyl 4-(3,4,5-Trimethoxyphenyl)benzoate

3,4,5-Trimethoxyphenylboronic acid (2.01 g) and ethyl 4-bromobenzoate (2.29 g) were condensed in the same manner as described in Preparation Example 1 to give the title compound.

Yield: 2.99 g (95%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.42 (t, 3H, J=7.2 Hz), 3.90 (s, 3H), 3.94 (s, 6H), 4.38 (q, 2H, J=7.2 Hz), 6.81 (s, 2H), 7.62 (d, 2H, J=8.2 Hz), 8.10 (d, 2H, J=8.2 Hz).

PREPARATION EXAMPLE 67 Synthesis of 4-(3,4,5-Trimethoxyphenyl)benzyl Alcohol

Ethyl 4-(3,4,5-trimethoxyphenyl)benzoate (2.99 g) was treated in the same manner as described in Preparation Example 2 to give the title compound.

Yield: 1.83 g (71%).

PREPARATION EXAMPLE 68 Synthesis of 4-(3,4,5-Trimethoxyphenyl)benzyl Chloride

4-(3,4,5-Trimethoxyphenyl)benzyl alcohol (1.83 g) was treated in the same manner as describe in Preparation Example 3 to give the title compound.

Yield: 1.65 g (84%). ¹H-NMR (400 MHz, CDCl₃) δ: 3.90 (s, 3H), 3.93 (s, 6H), 4.65 (s, 2H), 6.77 (s, 2H), 7.46 (d, 2H, J=8.0 Hz), 7.55 (d, 2H, J=8.0 Hz).

EXAMPLE 26

 

Synthesis of 4-[N-(3,5-Dimethoxyphenyl)-N-[4-(3,4,5-trimethoxypheny)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

4-(3,5-Dimethoxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (148 mg) and 4-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a dihydrochloride which gave yellow powder of the title compound.

Yield: 35 mg (14%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ; 1.80-1.89 (m, 4H), 2.17 (br, 2H), 2.97 (d, 2H, J=10.5 Hz), 3.57 (s, 2H), 3.70 (s, 6H), 3.77-3.84 (m, 1H), 3.87 (s, 3H), 3.90 (s, 3H), 3.91 (s, 6H), 3.96 (s, 6H), 4.52 (s, 2H), 5.93 (s, 2H), 6.74 (s, 2H), 7.19-7.22 (m, 4H), 7.31 (d, 2H, J=8.2 Hz), 7.46 (d, 2H, J=8.2 Hz), 7.60 (s, 1H), 8.59 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 69 Synthesis of 4-(3,4-Methylenedioxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine

1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl-4-piperidone (1.40 g) and 3,4-methylenedioxyaniline (646 mg) were treated in the same manner as described in Preparation Example 29 to give the title compound.

Yield: 810 mg (43%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.63 (br, 2H), 2.02-2.60 (m, 4H), 2.80-3.15 (m, 2H), 3.25 (br, 1H), 3.70 (br, 2H), 3.88 (s, 3H), 3.96 (s, 6H), 5.83 (s, 2H), 6.02 (d, 1H, J=8.3 Hz), 6.22 (s, 1H), 6.61 (d, 1H, J=8.3 Hz), 7.18-7.28 (m, 3H), 7.64 (br, 1H), 8.60 (d, 1H, J=4.9 Hz).

EXAMPLE 27

 

Synthesis of 4-[N-(3,4-Methylenedioxyphenyl)-N-[[2-(3,4,5-trimethoxypheny)pyridin-3-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(3,4-Methylenedioxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (119 mg) and 3-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed in the same manner as described in Example 9. Yellow syrup obtained was converted to a trihydrochloroide to give the title compound as yellow powder.

Yield: 30 mg (14%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.45-2.25 (m, 6H), 2.90 (br, 2H), 3.40 (br, 1H), 3.55 (br, 2H), 3.87 (s, 3H), 3.88 (s, 9H), 3.93 (s, 6H), 4.28 (s, 2H), 5.82 (s, 2H), 6.10 (br, 1H), 6.28 (s, 1H), 6.58 (d, 1H, J=8.4 Hz), 6.67 (s, 2H), 7.12-7.30 (m, 4H), 7.52 (br, 1H), 7.75 (br, 1H), 8.51 (br, 1H), 8.57 (br, 1H).

EXAMPLE 28

 

Synthesis of 4-[N-(3,4-Methylenedioxyphenyl)-N-[2-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]metyl]piperidine Dihydrochloride

4-(3,4-Methylenedioxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (119 mg) and 2-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed in the same manner as described in Example 9. A free base obtained was converted to a dihydrochloroide to give the title compound as yellow powder.

Yield: 13 mg (6%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.61 (br, 2H), 1.78 (br, 2H), 2.10 (br, 2H), 2.91 (br, 2H), 3.50-3.54 (m, 3H), 3.87 (s, 6H), 3.90 (s, 3H), 3.92 (s, 3H), 3.99 (s, 6H), 4.26 (s, 2H), 5.82 (s, 2H), 6.12 (d, 1H, J=8.6 Hz), 6.32 (s, 1H), 6.53 (s, 2H), 6.62 (d, 1H, J=8.6 Hz), 7.17-7.26 (m, 6H), 7.42 (br, 1H), 7.55 (s, 1H), 8.58 (d, 1H, J=4.9 Hz).

EXAMPLE 29

 

Synthesis of 4-[N-(3,4-Methylenedioxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(3,4-Methylenedioxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (119 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl) pyridine (114 mg) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a trihydrochloride which gave the title compound as yellow powder.

Yield: 52 mg (25%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.60-1.95 (m, 4H), 2.20 (br, 2H), 3.00 (br, 2H), 3.58 (br, 3H), 3.86 (s, 3H), 3.87 (s, 3H), 3.91 (s, 6H), 3.94 (s, 6H), 4.41 (s, 2H), 5.82 (s, 2H), 6.17 (d, 1H, J=8.4 Hz), 6.39 (s, 1H), 6.62 (d, 1H, J=8.4 Hz), 7.12-7.13 (m, 3H), 7.18 (d, 1H, J=4.1 Hz), 7.23 (br, 2H), 7.54 (br, 2H), 8.51 (d, 1H, J=5.1 Hz), 8.57 (d, 1H, J=4.9 Hz).

EXAMPLE 30

 

Synthesis of 4-[N-(3,4-Methylenedioxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

4-(3,4-Methylenedioxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (119 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a dihydrochloride which gave the title compound as yellow powder.

Yield: 58 mg (29%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.60-1.97 (m, 4H), 2.15 (br, 2H), 3.00 (br, 2H), 3.58 (br, 3H), 3.86 (s, 3H), 3.88 (s, 9H), 3.94 (s, 6H), 4.43 (s, 2H), 5.81 (s, 2H), 6.21 (br, 1H), 6.42 (s, 1H), 6.62 (d, 1H, J=8.4 Hz), 6.69 (s, 2H), 7.18 (d, 1H, J=4.9 Hz), 7.22-7.39 (m, 6H), 7.60 (br, 1H), 8.57 (d, 1H, J=4.9 Hz).

EXAMPLE 31

 

Synthesis of 4-[N-(3,4-Methylenedioxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(3,4-Methylenedioxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (119 mg) and 5-chloromethyl-2-(3,4,5-trimethoxyphenyl) pyridine (114 mg) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a trihydrochloride which gave the title compound as yellow powder.

Yield: 69 mg (27%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.71-1.88 (m, 4H), 2.14 (d, 2H, J=11.2 Hz), 2.97 (d, 2H, J=11.5 Hz), 3.45-3.52 (m, 1H), 3.56 (s, 2H), 3.89 (s, 3H), 3.90 (s, 3H), 3.94 (s, 6H), 3.96 (s, 6H), 4.12 (s, 2H), 5.85 (s, 2H), 6.24 (dd, 1H, J=8.5 Hz, 2.5 Hz), 6.45 (d, 1H, J=2.4 Hz), 6.64 (d, 1H, J=8.5 Hz), 7.20-7.21 (m, 1H), 7.21 (s, 2H), 7.23 (s, 2H), 7.58-7.65 (m, 3H), 8.57 (d, 1H, J=1.5 Hz), 8.59 (d, 1H, J=4.9 Hz).

EXAMPLE 32

 

Synthesis of 4-[N-(3,4-Methylenedioxyphenyl)-N-[4-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

4-(3,4-Methylenedioxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (119 mg) and 4-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed by the same manner as described in Example 9. Yellow oil of a free base was converted to a dihydrochloride which gave the title compound as yellow powder.

Yield: 29 mg (14%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ; 1.62-2.00 (m, 4H), 2.20 (br, 2H), 2.99 (br, 2H), 3.58 (br, 3H), 3.86 (s, 3H), 3.87 (s, 3H), 3.88 (s, 6H), 3.89 (s, 6H), 4.41 (s, 2H), 5.82 (s, 2H), 6.19 (d, 1H, J=8.6 Hz), 6.39 (s, 1H), 6.63 (d, 1H, J=8.4 Hz), 6.72 (s, 2H), 7.18 (d, 1H, J=5.1 Hz), 7.23 (s, 2H), 7.29 (d, 2H, J=8.0 Hz), 7.43 (d, 2H, J=8.2 Hz), 7.60 (br, 1H), 8.57 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 70 Synthesis of 4-[N-Methyl-N-[(2-nitrobenzene)sulfonyl]aminomethyl]-2-(3,4,5-trimethoxyphenyl)pyridine

4-Chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (232 mg), N-methyl-2-nitrobenzenesulfonamide (171 mg) and potassium carbonate (138 mg) were suspended in acetonitrile (10 mL). The mixture was stirred at room temperature overnight and evaporated. To the residue was added chloroform and water. The organic layer was separated, washed with saturated aqueous sodium hydrogencarbonate and brine, dried over anhydrous magnesium sulfate and evaporated to give the title compound.

Yield: 362 mg (97.0%).

PREPARATION EXAMPLE 71 Synthesis of 4-(Methylaminomethyl)-2-(3,4,5-trimethoxyphenyl)pyridine

To a suspension of 4-[N-methyl-N-[(2-nitrobenzene)sulfonyl]aminomethyl]-2-(3,4,5-trimethoxyphenyl)pyridine (691 mg) and potassium carbonate (203 mg) in acetonitrile (20 mL) was added thiophenol (228 μL). The mixture was stirred at 50° C. overnight and evaporated. To the residue was added chloroform and water. The organic layer was separated, washed with saturated aqueous sodium hydrogencarbonate and brine, dried over anhydrous magnesium sulfate and evaporated. The residue was subjected to a column of silica gel using chloroform-methanol (40:1) and then chloroform-methanol (10:1) as eluents. Fractions containing the product were collected and evaporated to give the title compound.

Yield: 356 mg (84%).

EXAMPLE 33

 

Synthesis of 4-[N-Methyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]aminocarbonyl]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Maleate

1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine-4-caroxylic acid (98 mg) and 4-(methylaminomethyl)-2-(3,4,5-trimethoxyphenyl)pyridine (73 mg) were condensed by the same manner as described in Example 1 giving a maleate of the title compound as white powder.

Yield: 145 mg (75%). ¹H-NMR (400 MHz, measured as a maleate, DMSO-d₆) δ: 1.89-1.97 (m, 4H), 2.75-2.96 (m, 3H), 3.03 (s, 3H), 3.27 (d, 2H, J=12.0 Hz), 3.78 (s, 3H), 3.79 (s, 3H), 3.87 (s, 6H), 3.90 (s, 6H), 4.09 (s, 2H), 4.64 (s, 2H), 6.14 (s, 2H), 7.09 (d, 1H, J=5.0 Hz), 7.33 (s, 2H), 7.37 (d, 1H, J=5.0 Hz), 7.38 (s, 2H), 7.65 (s, 1H), 7.90 (s, 1H), 8.57 (d, 1H, J=5.0 Hz), 8.67 (d, 1H, J=5.0 Hz).

PREPARATION EXAMPLE 72 Synthesis of (3S)-1-(tert-Butoxycarbonyl)-3-[N-[(2-nitrobenzene)sulfonyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]pyrrolidine

(3S)-1-(tert-Butoxycarbonyl)-3[(2-nitrobenzene)sulfonylamino]pyrrolidine (72 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (57 mg) were condensed in the same manner as described in Example 2 to give colorless amorphous of the title compound.

Yield: 103 mg (85%).

PREPARATION EXAMPLE 73 Synthesis of (3S)-3-[N-[(2-Nitrobenzene)sulfonyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]pyrrolidine

(3S)-1-(tert-butoxycarbonyl)-3-[N-[(2-nitrobenzene)sulfonyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]pyrrolidine (103 mg) was treated in the same manner as described in Preparation Example 12 to give yellow amorphous of the title compound.

Yield: 72 mg (84%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.66-1.75 (m, 1H), 2.03-2.05 (m, 1H), 2.78-2.85 (m, 2H), 3.00-3.10 (m, 2H), 3.39 (br, 1H), 3.90 (s, 3H), 3.96 (s, 6H), 4.59-4.67 (m, 1H), 4.70 (s, 2H), 7.13-7.18 (m, 1H), 7.20 (s, 2H), 7.52-7.64 (m, 4H), 7.95 (dd, 1H, J=7.9 Hz, 1.1 Hz), 8.52 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 74 Synthesis of (3S)-3-[N-[(2-Nitrobenzene)sulfonyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]pyrrolidine

(3S)-3-[N-[(2-Nitrobenzene)sulfonyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]pyrrolidine (72 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (40 mg) were treated in the same manner as described in Example 2 to give a yellow amorphous of the title compound.

Yield: 97 mg (91%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.59 (br, 1H), 1.80-1.90 (m, 1H), 2.20-2.30 (m, 2H), 2.55 (dd, 1H, J=10.5 Hz, 8.2 Hz), 2.78 (dd, 1H, J=10.6 Hz, 3.2 Hz), 2.87 (t, 1H, J=7.2 Hz), 3.50 (d, 1H, J=13.7 Hz), 3.64 (d, 1H, J=13.7 Hz), 3.89 (s, 3H), 3.90 (s, 3H), 3.92 (s, 6H), 3.93 (s, 6H), 4.83 (d, 2H, J=4.5 Hz), 7.07 (d, 1H, J=5.1 Hz), 7.10 (d, 1H, J=4.9 Hz), 7.15 (s, 2H), 7.17 (s, 2H), 7.41-7.45 (m, 1H), 7.50-7.55 (m, 3H), 7.61 (s, 1H), 7.81 (d, 1H, J=7.4 Hz), 8.45 (d, 1H, J=4.9 Hz), 8.51 (d, 1H, J=5.1 Hz).

EXAMPLE 34

 

Synthesis of (3S)-1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-3-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methylamino]pyrrolidine Trihydrochloride

(3S)-3-[N-[(2-nitrobenzene)sulfonyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]pyrrolidine (97 mg) was treated in the same manner as described in Preparation Example 11 to give yellow amorphous of the title compound, which was converted to a trihydrochloride.

Yield: 80 mg (89%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.71 (br, 2H), 2.19-2.21 (m, 1H), 2.52-2.55 (m, 2H), 2.73-2.77 (m, 2H), 3.39 (br, 1H), 3.66 (d, 1H, J=13.7 Hz), 3.71 (d, 1H, J=13.7 Hz), 3.82 (s, 2H), 3.90 (s, 6H), 3.95 (s, 12H), 7.18-7.21 (m, 2H), 7.23 (s, 2H), 7.24 (s, 2H), 7.63 (s, 2H), 8.59 (d, 1H, J=4.3 Hz), 8.60 (d, 1H, J=4.3 Hz).

EXAMPLE 35

 

Synthesis of 4-[3-(3,4,5-Trimethoxyphenyl)benzoylamino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Maleate

3-(3,4,5-trimethoxyphenyl)benzoic acid (69 mg) and 4-amino-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (114 mg) were condensed in the same manner as described in Example 1. The title compound was obtained after converting the product to a maleate.

Yield: 100 mg (56%). ¹H-NMR (400 MHz, measured as a maleate, DMSO-d₆) δ: 1.85-2.10 (m, 4H), 2.77-2.93 (m, 2H), 3.20-3.31 (m, 2H), 3.77 (s, 3H, 3.79 (s, 3H), 3.89 (s, 6H), 3.91 (s, 6H), 3.98-4.07 (m, 1H), 4.13 (s, 2H), 6.15 (s, 2H), 6.94 (s, 2H), 7.40-7.52 (m, 4H), 7.73-7.80 (m, 2H), 8.02-8.10 (m, 3H), 8.67-8.68 (m, 1H).

EXAMPLE 36

 

Synthesis of 4-[N-Methyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Tetrahydrochloride

4-(methylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (2.67 g) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (2.12 g) were condensed in the same manner as described in Example 2. The title compound was obtained after converting a free base to a tetrahydrochloride.

Yield: 2.55 g (46%).

¹H-NMR (400 MHz, measured as a maleate, DMSO-d₆δ: 1.85-2.10 (m, 4H), 2.77-2.93 (m, 2H), 3.20-3.31 (m, 2H) 3.77 (s, 3H), 3.79 (s, 3H), 3.89 (s, 6H), 3.91 (s, 6H), 3.98-4.07 (m, 1H), 4.13 (s, 2H), 6.15 (s, 2H), 6.94 (s, 2H), 7.40-7.52 (m, 4H), 7.73-7.80 (m, 2H), 8.02-8.10 (m, 3H), 8.67-8.68 (m, 1H).

PREPARATION EXAMPLE 75 Synthesis of 1-(Ethoxycarbonyl)-4-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methylamino]piperidine

4-Amino-1-(ethoxycarbonyl)piperidine (341 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (300 mg) were condensed in the same manner as described in Example 2 to give the title compound.

Yield: 438 mg (theoretical yield). ¹H-NMR (400 MHz, CDCl₃) δ: 1.25 (t, 3H, J=7.1 Hz), 1.27-1.34 (m, 2H), 1.60 (br, 1H), 1.90 (d, 2H, J=l10.9 Hz), 2.67-2.72 (m, 1H), 2.87 (t, 2H, J=11.5 Hz), 3.90 (s, 3H), 3.91 (br, 2H), 3.96 (s, 6H), 4.09 (br, 2H), 4.12 (q, 2H, J=7.0 Hz), 7.21 (d, 1H, J=3.5 Hz), 7.24 (s, 2H), 7.65 (s, 1H), 8.59 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 76 Synthesis of 1-(Ethoxycarbonyl)-4-[N-methyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

To a solution of 1-(ethoxycarbonyl)-4-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methylamino]piperidine (438 mg) was treated in the same manner as described in Preparation Example 11 to give the title compound as yellow syrup.

Yield: 235 mg (52%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.26 (t, 3H, J=7.1 Hz), 1.42-1.57 (m, 2H), 1.82 (d, 2H, J=11.9 Hz), 2.24 (s, 3H), 2.59-2.65 (m, 1H), 2.75 (t, 2H, J=12.0 Hz), 3.65 (s, 2H), 3.90 (s, 3H), 3.97 (s, 6H), 4.13 (q, 2H, J=7.0 Hz), 4.23 (br, 2H), 7,22 (dd, 1H, J=5.0 Hz, 1.3 Hz), 7.24 (s, 2H), 7.63 (s, 1H), 8.59 (d, 1H, J=4.5 Hz).

PREPARATION EXAMPLE 77 Synthesis of 4-[N-Methyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

To a solution of 1-(ethoxycarbonyl)-4-[N-methyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (100 mg) in ethanol (2 mL) was added 4 M sodium hydroxide (8 mL). The mixture was refluxed overnight and extracted with chloroform. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate and evaporated. The residue was subjected to a column of silica gel and liquid chromatography was performed using chloroform-methanol (20:1) to give the title compound as yellow syrup.

Yield: 73 mg (88%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.50-1.55 (m, 2H), 1.84 (d, 2H, J=12.0 Hz), 1.99 (br, 1H), 2.25 (s, 3H), 2.55-2.63 (m, 3H), 3.16 (d, 2H, J=12.2 Hz), 3.65 (s, 2H), 3.90 (s, 3H), 3.97 (s, 6H), 7.22 (d, 1H, J=6.1 Hz), 7.24 (s, 2H), 7.64 (s, 1H), 8.58 (d, 1H, J=5.1 Hz).

EXAMPLE 37

 

Synthesis of 4-[N-Methyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Tetrahydrochloride

4-[N-methyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (73 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (58 mg) were condensed in the same manner as described in Example 2. The title compound was obtained after converting a free base to a tetrahydrochloride.

Yield: 126 mg (84%).

EXAMPLE 38

 

Synthesis of 4-[N-Methyl-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Difumarate

4-(methylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (111 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (88 mg) were condensed in the same manner as described in Example 2. The title compound was obtained as white powder after converting a free base to a difumarate.

Yield: 59 mg (46%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.70-1.77 (m, 2H), 1.85-1.87 (m, 2H), 2.03-2.08 (m, 2H), 2.27 (s, 3H), 2.55-2.59 (m, 1H), 2.98 (d, 2H, J=1l.3 Hz), 3.56 (s, 2H), 3.69 (s, 2H), 3.89 (s, 3H), 3.90 (s, 3H), 3.93 (s, 6H), 3.98 (s, 6H), 6.79 (s, 2H), 7.22 (d, 1H, J=4.9 Hz), 7.28 (s, 2H), 7.31 (d, 1H, J=7.6 Hz), 7.38 (t, 1H, J=7.4 Hz), 7.45 (d, 1H, J=7.6 Hz), 7.51 (s, 1H), 7.63 (s, 1H), 8.60 (d, 1H, J=5.1 Hz).

EXAMPLE 39

 

Synthesis of 4-[N-Methyl-N-[[2-(3,5-dimethoxy-4-hydroxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,5-dimethoxy-4-hydroxyphenyl)pyridin-4-yl]methyl]piperidine Tetrahydrochloride

To an ice-cooled solution of 4-[N-methyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (100 mg) in dichloromethane (5 mL) was added iodotrimethylsilane (173 μL). The mixture was stirred at 0° C. for 2 hours and then at room temperature overnight. A small amount of water, ethyl acetate and saturated aqueous sodium hydrogencarbonate were added to the mixture at 0° C. and the organic layer was separated. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and evaporated. The residue was applied to a preparative TLC using chloroform-ammonia saturated methanol (15:1) to give a free base of the title compound which was converted to a tetrahydrochloride by the conventional method.

Yield: 50 mg (52.3%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.68-1.89 (m, 4H), 2.03-2.12 (m, 2H), 2.26 (s, 3H), 2.48-2.60 (m, 1H), 2.98-3.05 (m, 2H), 3.57 (s, 2H), 3.65 (s, 2H), 3.94 (s, 6H), 3.95 (s, 6H), 7.16-7.19 (m, 2H), 7.26 (s, 2H), 7.27 (s, 2H), 7.62-7.68 (m, 2H), 8.56 (d, 1H, J=5.3 Hz), 8.58 (d, 1H, J=5.2 Hz).

PREPARATION EXAMPLE 78 Synthesis of 1-(Ethoxycarbonyl)-4-[N-ethyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

To a solution of 1-(ethoxycarbonyl)-4-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methylamino]piperidine (400 mg) in acetonitrile (5 mL) was added potassium carbonate (13 mg) and iodoethane (145 mg). The mixture was placed in sealed vessel and stirred at 80° C. for 2 hours. After removing the solvent in vacuo, ethyl acetate was added, washed with water and brine, dried over anhydrous sodium sulfate and evaporated. The residue was subjected to a column of silica gel using chloroform-methanol (30:1) as an eluent. Fractions containing the product were collected and evaporated to give the title compound as yellow syrup.

Yield: 242 mg (57%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.04 (t, 3H, J=7.1 Hz), 1.25 (t, 3H, J=7.1 Hz), 1.43-1.52 (m, 2H), 1.79 (d, 2H, J=11.5 Hz), 2.60 (q, 2H, J=7.0 Hz), 2.66-2.76 (m, 3H), 3.70 (s, 2H), 3.90 (s, 3H), 3.97 (s, 6H), 4.12 (q, 2H, J=7.0 Hz), 4.20 (br, 2H), 7.23 (s, 2H), 7.26 (d, 1H, J=5.7 Hz), 7.67 (s, 1H), 8.58 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 79 Synthesis of 4-[N-Ethyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

1-(ethoxycarbonyl)-4-[N-ethyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (242 mg) was treated in the same manner as described in Preparation Example 77 to give the title compound as yellow syrup.

Yield: 150 mg (74%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.03 (t, 3H, J=7.0 Hz), 1.43-1.52 (m, 2H), 1.70 (br, 1H), 1.79 (d, 2H, J=12.3 Hz), 2.53-2.67 (m, 5H), 3.13 (d, 2H, J=11.9 Hz), 3.71 (s, 2H), 3.90 (s, 3H), 3.97 (s, 6H), 7.24 (s, 2H), 7.27 (d, 1H, J=5.1 Hz), 7.68 (s, 1H), 8.57 (d, 1H, J=4.3 Hz).

EXAMPLE 40

 

Synthesis of 4-[N-Ethyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Tetrahydrochloride

4-[N-ethyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (65 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (50 mg) were condensed in the same manner as described in Example 2. The title compound was obtained after converting a free base to a tetrahydrochloride.

Yield: 121 mg (90%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.03 (t, 3H, J=7.1 Hz), 1.64-1.69 (m, 2H), 1.77 (d, 2H, J=10.7 Hz), 2.01 (t, 2H, J=10.8 Hz), 2.55-2.64 (m, 3H), 2.95 (d, 2H, J=1.l Hz), 3.53 (s, 2H), 3.71 (s, 2H), 3.90 (s, 6H), 3.97 (s, 12H), 7.20-7.27 (m, 6H), 7.60 (s, 1H), 7.68 (s, 1H), 8.57 (d, 1H, J=4.9 Hz), 8.59 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 80 Synthesis of 4-(Cyclohexylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine

1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-4-pieridone (400 mg) and cyclohexylamine (134 mg) were reacted in the same manner as described in Preparation Example 37 to give the title compound.

Yield: 342 mg (69%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.05-1.30 (m, 6H), 1.38-1.52 (m, 2H), 1.53-1.80 (m, 3H), 1.87 (br, 4H), 2.07 (t, 2H, J=10.7 Hz), 2.59(br, 2H), 2.86 (br, 2H), 3.54 (s, 2H), 3.90 (s, 3H), 3.97 (s, 6H), 7.19 (d, 1H, J=4.9 Hz), 7.24 (s, 2H), 7.64 (s, 1H), 8.58 (d, 1H, J=4.9 Hz).

EXAMPLE 41

 

Synthesis of 4-[N-Cyclohexyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Tetrahydrochloride

4-(Cyclohexylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (342 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (252 mg) were reacted in the same manner as described in Preparation Example 6. The title compound was obtained after converting the product to a tetrahydrochloride.

Yield: 55 mg (8%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.00-1.39 (m, 6H), 1.58-1.88 (m, 8H), 2.07 (br, 2H), 2.61 (br, 2H), 2.96 (br, 2H), 3.57 (br, 2H), 3.85 (s, 2H), 3.90 (s, 3H), 3.91 (s, 3H), 3.97 (s, 12H), 7.19-7.28 (m, 6H), 7.70 (br, 2H), 8.56 (d, 1H, J=5.1 Hz), 8.60 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 81 Synthesis of 4-Anilino-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine

1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone (1.1 g) and aniline (344 mg) were reacted in the same manner as described in Preparation Example 37 to give the title compound.

Yield: 1.09 g (81%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.53 (br, 2H), 2.02-2.13 (m, 2H), 2.16-2.32 (m, 2H), 2.86 (br, 2H), 3.32 (br, 1H), 3.59 (s, 2H), 3.88 (s, 3H), 3.95 (s, 6H), 6.57 (d, 2H, J=8.6 Hz), 6.66 (t, 1H, J=7.3 Hz), 7.14 (t, 2H, J=7.9 Hz), 7.20-7.24 (m, 5H), 7.65 (br, 1H), 8.59 (d, 1H, J=5.1 Hz).

EXAMPLE 42

 

Synthesis of 4-[N-Phenyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-Anilino-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (1.64 g) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (1.64 g) were reacted in the same manner as described in Preparation Example 9. The title compound was obtained after converting the product to a trihydrochloride.

Yield: 635 mg (20%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.60-2.00 (m, 4H), 2.10-2.35 (m, 2H), 2.99 (br, 2H), 3.58 (br, 3H), 3.86 (s, 3H), 3.88 (s, 3H), 3.90 (s, 6H), 3.94 (s, 6H), 4.52 (s, 2H), 6.66-6.78 (m, 3H), 7.13-7.28 (m, 8H), 7.54 (br, 2H), 8.53 (d, 1H, J=5.1 Hz), 8.58 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 82 Synthesis of 1-[[2-(4-Chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone Ethylene Ketal

4-Piperidone ethylene ketal (573 mg) and 2-(4-chloro-3,5-dimetoxyphenyl)-4-chloromethylpyridine (1.19 g) were condensed in the same manner as described in Example 2 to give the title compound.

Yield: 1.67 g (theoretical amount). ¹H-NMR (400 MHz, CDCl₃) δ: 1.78 (t, 4H, J=5.6 Hz), 2.58 (br, 4H), 3.61 (s, 2H), 3.67 (s, 4H), 4.02 (s, 6H), 7.25-7.29 (m, 3H), 7.68 (s, 1H), 8.61 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 83 Synthesis of 1-[[2-(4-Chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone

1-[[2-(4-Chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone ethylene ketal (1.67 g) was treated in the same manner as described in Preparation Example 23 to give the title compound.

Yield: 1.29 g (89%). ¹H-NMR (400 MHz, CDCl₃) δ: 2.50 (t, 4H, J=5.8 Hz), 2.81 (t, 4H, J=5.8 Hz), 3.71 (s, 2H), 4.02 (s, 6H), 7.26 (s, 2H), 7.33 (d, 1H, J=4.3 Hz), 7.70 (s, 1H), 8.66 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 84 Synthesis of 4-Anilino-1-[[2-(4-chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]piperidine

1-[[2-(4-Chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone (600 mg) and aniline (0.18 mL) were reacted in the same manner as described in Preparation Example 37 to give the title compound.

Yield: 465 mg (63%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.49-1.69 (m, 2H), 2.08 (d, 2H, J=7.8 Hz), 2.23 (t, 2H, J=9.3 Hz), 2.87 (d, 2H, J=7.8 Hz), 3.34 (br, 1H), 3.60 (s, 2H), 4.02 (s, 6H), 6.60 (d, 2H, J=7.6 Hz), 6.69 (t, 1H, J=7.3 Hz), 7.10-7.20 (m, 2H), 7.20-7.30 (m, 3H), 7.67 (s, 1H), 8.62 (d, 1H, J=5.2 Hz).

EXAMPLE 43

 

Synthesis of 1-[[2-(4-Chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[[2-(4-chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]-N-phenylamino]piperidine Trihydrochloride

4-Anilino-1-[[2-(4-chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]piperidine (230 mg) and 2-(4-chloro-3,5-dimethoxyphenyl)-4-chloromethylpyridine (157 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a trihydrochloride.

Yield: 104 mg (24%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.70-1.85 (m, 4H), 2.20 (t, 2H, J=2.3 Hz), 3.00 (d, 2H, J=1.3 Hz), 3.59 (s, 2H), 3.96 (s, 6H), 4.00 (s, 6H), 4.56 (s, 2H), 6.65-6.78 (m, 3H), 7.16 (s, 2H), 7.18-7.28 (m, 6H), 7.59 (s, 1H), 7.62 (s, 1H), 8.57 (d, 1H, J=5.1 Hz), 8.57 (d, 1H, J=4.8 Hz).

PREPARATION EXAMPLE 85 Synthesis of 4-(p-Anisidino)-1-[[2-(4-chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]piperidine

1-[[2-(4-Chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone (690 mg) and p-anisidine (283 mg) were reacted in the same manner as described in Preparation Example 37 to give the title compound.

Yield: 646 mg (72%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45-1.55 (m, 2H), 2.05 (d, 2H, J=11.7 Hz), 2.20 (t, 2H, J=11.2 Hz), 2.87 (d, 2H, J=11.7 Hz), 3.20-3.35 (m, 1H), 3.59 (s, 2H), 3.74 (s, 3H), 4.02 (s, 6H), 6.58 (d, 2H, J=8.7 Hz), 6.77 (d, 2H, J=8.7 Hz), 7.25-7.28 (m, 3H), 7.67 (s, 1H), 8.62 (d, 1H, J=4.9 Hz).

EXAMPLE 44

 

Synthesis of 1-[[2-(4-Chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[[2-(4-chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine Trihydrochloride

4-p-Anisidino)-1-[[2-(4-chloro-3,5-dimethoxyphenyl)pyridin-4-yl]methyl]piperidine (271 mg) and 2-(4-chloro-3,5-dimethoxyphenyl)-4-chloromethylpyridine (173 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a trihydrochloride.

Yield: 324 mg (67%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.65-1.90 (m, 4H), 2.16 (t, 2H, J=10.4 Hz), 2.97 (d, 2H, J=7.5 Hz), 3.54-3.60 (m, 1H), 3.58 (s, 2H), 3.73 (s, 3H), 3.97 (s, 6H), 4.00 (s, 6H), 4.46 (s, 2H), 6.74 (d, 2H, J=9.4 Hz), 6.79 (d, 2H, J=9.4 Hz), 7.16 (s, 2H), 7.20-7.29 (m, 4H), 7.59 (s, 1H), 7.62 (s, 1H), 8.56 (d, 1H, J=4.8 Hz), 8.60 (d, 1H, J=4.8 Hz).

PREPARATION EXAMPLE 86 Synthesis of 4-(3-Methylthioanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine

1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone (1.40 g) and 3-methylthioaniline (655 mg) were reacted in the same manner as described in Preparation Example 37 to give the title compound.

Yield: 1.01 g (54%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.44-1.60 (m, 2H), 1.98-2.10 (m, 2H), 2.23 (br, 2H), 2.42 (s, 3H), 2.88 (br, 2H), 3.30 (br, 1H), 3.59 (s, 2H), 3.88 (s, 3H), 3.95 (s, 6H), 6.35 (d, 1H, J=7.6 Hz), 6.47 (s, 1H), 6.55 (d, 1H, J=8.6 Hz), 7.05 (t, 1H, J=7.9 Hz), 7.20 (d, 1H, J=4.9 Hz), 7.24 (s, 2H), 7.68 (br, 1H), 8.58 (d, 1H, J=4.9 Hz).

EXAMPLE 45

 

Synthesis of 4-[N-(3-Methylthiophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-3-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(3-Methylthioanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (143 mg) and 3-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a trihydrochloride.

Yield: 45 mg (18%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.58-1.71 (s, 2H), 1.79 (d, 2H, J=10.7 Hz), 2.16 (t, 2H, J=11.2 Hz), 2.38 (s, 3H), 2.96 (d, 2H, J=11.2 Hz), 3.56 (s, 3H), 3.68-3.97 (m, 1H), 3.90 (s, 3H), 3.92 (s, 9H), 3.96 (s, 9H), 4.42 (s, 2H), 6.45 (d, 1H, J=8.3 Hz), 6.52 (s, 1H), 6.61 (d, 1H, J=7.3 Hz), 6.74 (s, 2H), 7.11 (t, 1H, J=8.1 Hz), 7.15-7.26 (m, 4H), 7.54 (s, 1H), 7.68 (d, 1H, J=7.8 Hz), 8.53 (d, 1H, J=3.2 Hz), 8.59 (d, 1H, J=4.8 Hz).

EXAMPLE 46

 

Synthesis of 4-[N-(3-Methylthiophenyl)-N-[2-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

4-(3-Methylthioanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (143 mg) and 2-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a dihydrochloride.

Yield: 51 mg (23%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.56-1.73 (m, 2H), 1.78-1.87 (m, 2H), 2.10-2.20 (m, 2H), 2.38 (s, 3H), 2.91-2.98 (m, 2H), 3.55 (s, 2H), 3.70-3.80 (m, 1H), 3.88 (s, 6H), 3.90 (s, 3H), 3.92 (s, 3H), 3.96 (s, 6H), 4.35 (s, 2H), 6.47 (d, 1H, J=8.2 Hz), 6.53-6.62 (m, 5H), 7.09 (t, 1H, J=8.0 Hz), 7.18-7.40 (m, 6H), 7.54 (s, 1H), 8.58 (d, 1H, J=4.7 Hz).

EXAMPLE 47

 

Synthesis of 4-[N-(3-Methylthiophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Fumarate

4-(3-Methylthioanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (143 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as white powder after converting a free base to a fumarate.

Yield: 14 mg (5%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.76-1.86 (m, 5H), 2.17-2.23 (m, 2H), 2.39 (s, 3H), 2.97-3.00 (m, 2H), 3.58 (s, 2H), 3.89 (s, 3H), 3.90 (s, 3H), 3.93 (s, 6H), 3.96 (s, 6H), 4.54 (s, 2H), 6.47-6.50 (m, 1H), 6.63 (s, 1H), 6.64 (s, 1H), 7.10-7.15 (m, 2H), 7.15 (s, 2H), 7.20-7.21 (m, 1H), 7.22 (s, 2H), 7.55 (s, 1H), 7.59 (s, 1H), 8.56 (d, 1H, J=5.1 Hz), 8.59 (d, 1H, J=5.1 Hz).

EXAMPLE 48

 

Synthesis of 4-[N-(3-Methylthiophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

4-(3-Methylthioanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (143 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a dihydrochloride.

Yield: 60 mg (24%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.65-1.91 (m, 4H), 2.18 (t, 2H, J=10.5 Hz), 2.38 (s, 3H), 2.97 (d, 2H, J=10.9 Hz), 3.58 (s, 2H), 3.70-3.85 (m, 1H), 3.88 (s, 3H), 3.89 (s, 6H), 3.90 (s, 3H), 3.96 (s, 6H), 4.56 (s, 2H), 6.52 (d, 1H, J=8.4 Hz), 6.59 (d, 1H, J=7.6 Hz), 6.65 (s, 1H), 6.72 (s, 2H), 7.10 (t, 2H, J=8.0 Hz), 7.19-7.25 (m, 4H), 7.31-7.42 (m, 3H), 7.60 (s, 1H), 8.59 (d, 1H, J=7.8 Hz).

EXAMPLE 49

 

Synthesis of 4-[N-(3-Methylthiophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(3-Methylthioanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (143 mg) and 5-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a trihydrochloride.

Yield: 22 mg (9%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.50-2.05 (m, 4H), 2.20 (br, 2H), 2.37 (s, 3H), 3.05 (br, 2H), 3.50-3.70 (br, 3H), 3.86 (s, 3H), 3.87 (s, 3H), 3.92 (s, 6H), 3.95 (s, 6H), 4.52 (s, 2H), 6.49 (d, 1H, J=8.3 Hz), 6.62 (br, 2H), 7.09 (t, 1H, J=8.2 Hz), 7.18-7.30 (m, 6H), 7.58 (s, 2H), 8.54 (br, 1H), 8.60 (br, 1H).

EXAMPLE 50

 

Synthesis of 4-[N-(3-Methylthiophenyl)-N-[4-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

4-(3-Methylthioanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (143 mg) and 4-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a dihydrochloride.

Yield: 57 mg (22%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.58-1.83 (m, 4H), 2.20 (t, 2H, J=11.3 Hz), 2.39 (s, 3H), 2.98 (d, 2H, J=11.1 Hz), 3.58 (s, 2H), 3.88 (s, 3H), 3.90 (s, 3H), 3.91 (s, 6H), 3.96 (s, 6H), 4.53 (s, 2H), 6.51 (dd, 1H, J=8.4 Hz, 2.4 Hz), 6.60 (d, 1H, J=8.0 Hz), 6.64 (s, 1H), 6.75 (s, 2H), 7.10 (t, 1H, J=8.1 Hz), 7.24-7.33 (m, 4H), 7.47 (d, 2H, J=8.0 Hz), 7.61 (s, 1H), 8.59 (d, 1H, J=5.0 Hz).

PREPARATION EXAMPLE 87 Synthesis of 4-Propargylamino-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine

1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone (400 mg) and propargylamine (80 mg) were reacted in the same manner as described in Preparation Example 25 to give the title compound.

Yield: 227 mg (63%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.38-1.51 (m, 2H), 1.83-1.86 (m, 3H), 2.10-2.15 (m, 2H), 2.21 (s, 1H), 2.74 (br, 1H), 2.83-2.87 (m, 2H), 3.45 (s, 2H), 3.56 (s, 2H), 3.89 (s, 3H), 3.96 (s, 6H), 7.19 (d, 1H, J=4.9 Hz), 7.24 (s, 2H), 7.65 (s, 1H), 8.58 (d, 1H, J=4.9 Hz).

EXAMPLE 51

 

Synthesis of 4-[N-Propargyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Tetrahydrochloride

4-Proargylamino-1-[[2-(3,4,5,-trimethoxypheny)pyridin-4-yl]methyl]piperidine (227 mg) and 4-chloromethyl-2-(3,4,5-trimethoxypheny)pyridin (226 mg) were condensed in the same manner as describe in Example 9. The title compound was obtained as yellow powder after converting a free base to a tetrahydrochloride.

Yield: 128 mg (23%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.48-2.40 (m, 7H), 2.72 (br, 1H), 3.02 (br, 2H), 3.39 (s, 2H), 3.64 (br, 2H), 3.84 (s, 2H), 3.91 (s, 6H), 3.98 (s, 6H), 3.99 (s, 6H), 7.22-7.29 (m, 6H), 7.66 (br, 2H), 8.60 (d, 1H, J=4.9 Hz), 8.62 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 88 Synthesis of 4-(5-Indanylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine

1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone (1.40 g) and 5-aminoindan (680 mg) were reacted in the same manner as described in Preparation Example 37 to give the title compound.

Yield: 1.22 g (59%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.40-1.57 (m, 2H), 2.00-2.15 (m, 5H), 2.19-2.25 (m, 2H), 2.77-2.93 (m, 6H), 3.30 (br, 1H), 3.58 (s, 2H), 3.91 (s, 3H), 3.97 (s, 6H), 6.41 (d, 1H, J=8.0 Hz), 6.52 (s, 1H), 7.01 (d, 1H, J=8.0 Hz), 7.21-7.26 (m, 3H), 7.64 (s, 1H), 8.60 (d, 1H, J=4.9 Hz).

EXAMPLE 52

 

Synthesis of 4-[N-(Indan-5-yl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-3-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(5-Indanylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (142 mg) and 3-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a trihydrochloride.

Yield: 90 mg (41%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.54-1.67 (m, 2H), 1.74-1.83 (m, 2H), 1.98-2.07 (m, 2H), 2.09-2.98 (m, 2H), 3.55 (s, 2H), 3.64-3.74 (m, 1H), 3.90 (s, 3H), 3.91 (s, 6H), 3.92 (s, 3H), 3.96 (s, 6H), 4.41 (s, 2H), 6.49 (dd, 1H, J=8.2 Hz, 2.4 Hz), 6.59 (s, 1H), 6.74 (s, 2H), 7.04 (d, 1H, J=8.2 Hz), 7.15-7.20 (m, 2H), 7.22 (s, 2H), 7.54 (s, 1H), 7.77 (dd, 1H, J=7.8 Hz, 1.4 Hz), 8.52 (dd, 1H, J=4.7 Hz, 1.8 Hz), 8.59 (d, 1H, J=5.1 Hz).

EXAMPLE 53

 

Synthesis of 4-[N-(Indan-5-yl)-N-[2-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

4-(5-Indanylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (142 mg) and 2-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a dihydrochloride.

Yield: 115 mg (47%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.56-1.66 (m, 2H), 1.80-1.83 (m, 2H), 2.00-2.05 (m, 2H), 2.11-2.18 (m, 2H), 2.77-2.83 (m, 4H), 2.92-2.95 (m, 2H), 3.55 (s, 2H), 3.72 (br, 1H), 3.87 (s, 6H), 3.90 (s, 3H), 3.92 (s, 3H), 3.96 (s, 6H), 4.34 (s, 2H), 6.49 (d, 1H, J=8.3 Hz), 6.56 (s, 2H), 6.60 (s, 1H), 7.02 (d, 1H, J=8.3 Hz), 7.17-7.27 (m, 5H), 7.42-7.45 (m, 1H), 7.54 (s, 1H), 8.58 (d, 1H, J=4.9 Hz).

EXAMPLE 54

 

Synthesis of 4-[N-(Indan-5-yl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(5-Indanylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (142 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as white powder after converting a free base to a trihydrochloride.

Yield: 23 mg (9%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.60-1.95 (m, 4H), 2.00 (quint, 2H, J=7.3 Hz), 2.20 (br, 2H), 2.75-2.81 (m, 4H), 2.99 (br, 2H), 3.58 (br, 2H), 3.77 (s, 1H), 3.86 (s, 3H), 3.87 (s, 3H), 3.91 (s, 6H), 3.94 (s, 6H), 4.49 (s, 2H), 6.51 (d, 1H, J=8.3 Hz), 6.62 (s, 1H), 7.02 (d, 1H, J=8.0 Hz), 7.16 (s, 2H), 7.18-7.22 (m, 4H), 7.57 (br, 2H), 8.52 (d, 1H, J=4.9 Hz), 8.57 (d, 1H, J=4.9 Hz).

EXAMPLE 55 Synthesis of 4-[N-(Indan-5-yl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

4-(5-Indanylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (60 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a dihydrochloride.

Yield: 18 mg (19%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.60-1.95 (m, 4H), 2.00 (quint, 2H, J=7.2 Hz), 2.20 (br, 2H), 2.75-2.81 (m, 4H), 2.95 (br, 2H), 3.60 (br, 2H), 3.85 (br, 1H), 3.86 (s, 3H), 3.87 (s, 6H), 3.88 (s, 3H), 3.94 (s, 6H), 4.51 (s, 2H), 6.54 (d, 1H, J=8.2 Hz), 6.66 (s, 1H), 6.70 (s, 2H), 7.01 (d, 1H, J=8.4 Hz), 7.19 (d, 1H, J=4.9 Hz), 7.19-7.42 (m, 6H), 7.60 (br, 1H), 8.59 (br, 1H).

EXAMPLE 56

 

Synthesis of 4-[N-(Indan-5-yl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride

4-(5-Indanylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (143 mg) and 5-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a trihydrochloride.

Yield: 138 mg (63%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.71-1.91 (m, 4H), 1.98-2.06 (m, 2H), 2.13-2.22 (m, 2H), 2.76-2.84 (m, 4H), 2.94-3.05 (m, 2H), 3.57 (s, 2H), 3.69-3.78 (m, 1H), 3.89 (s, 3H), 3.90 (s, 3H), 3.94 (s, 6H), 3.96 (s, 6H), 4.50 (s, 2H), 6.57 (dd, 1H, J=8.2 Hz, 2.3 Hz), 6.67 (s, 1H), 7.04 (d, 1H, J=8.4 Hz), 7.20-7.22 (m, 1H), 7.22 (s, 2H), 7.23 (s, 2H), 7.57-7.62 (m, 1H), 7.60 (s, 1H), 7.65 (dd, 1H, J=8.2 Hz, 2.2 Hz), 8.58-8.62 (m, 2H).

EXAMPLE 57

 

Synthesis of 4-[N-(Indan-5-yl)-N-[4-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

4-(5-Indanylamino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (143 mg) and 4-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a dihydrochloride.

Yield: 95 mg (39%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.74-1.90 (m, 4H), 2.01-2.06 (m, 2H), 2.16-2.22 (m, 2H), 2.78-2.84 (m, 4H), 2.96-2.99 (m, 2H), 3.58 (s, 2H), 3.72 (br, 1H), 3.88 (s, 3H), 3.90 (s, 3H), 3.91 (s, 6H), 3.96 (s, 6H), 4.51 (s, 2H), 6.55 (d, 1H, J=8.3 Hz), 6.67 (s, 1H), 6.72 (s, 2H), 7.04 (d, 1H, J=8.3 Hz), 7.20 (d, 1H, J=5.1 Hz), 7.23 (s, 2H), 7.35 (d, 2H, J=8.1 Hz), 7.47 (d, 2H, J=8.1 Hz), 7.61 (s, 1H), 8.59 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 89 Synthesis of 4-(4-Butylanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine

1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-4-piperidone (1.24 g) and 4-butylaniline (149 mg) were reacted in the same manner as described in Preparation Example 37 to give the title compound.

Yield: 1.23 g (72%). ¹H-NMR (400 MHz, CDCl₃) δ: 0.82 (t, 3H, J=7.3 Hz), 1.20-1.30 (m, 2H), 1.38-1.50 (m, 4H), 1.92-2.25 (m, 4H), 2.40 (t, 2H, J=7.7 Hz), 2.77 (br, 2H), 3.21 (br, 1H), 3.50 (s, 2H), 3.82 (s, 3H), 3.89 (s, 6H), 6.45 (d, 2H, J=7.8 Hz), 6.89 (d, 2H, J=8.0 Hz), 7.13 (d, 1H, J=4.9 Hz), 7.18 (s, 2H), 7.58 (s, 1H), 8.52 (d, 1H, J=4.9 Hz).

EXAMPLE 58

 

Synthesis of 4-[N-(4-Butylphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-3-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(4-Butylanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (147 mg) and 3-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a trihydrochloride.

Yield: 58 mg (27%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 0.91 (t, 3H, J=7.3 Hz), 1.32-1.35 (m, 2H), 1.50-1.70 (m, 4H), 1.75 (br, 2H), 2.10-2.20 (m, 2H), 2.49 (t, 2H, J=7.6 Hz), 2.95 (br, 2H), 3.55 (s, 2H), 3.70 (br, 1H), 3.90 (s, 3H), 3.91 (s, 6H), 3.92 (s, 3H), 3.96 (s, 6H), 4.41 (s, 2H), 6.59 (d, 2H, J=8.8 Hz), 6.74 (s, 2H), 7.00 (d, 2H, J=8.6 Hz), 7.16-7.17 (m, 1H), 7.19 (d, 1H, J=4.9 Hz), 7.22 (s, 2H), 7.54 (s, 1H), 8.59 (d, 1H, J=7.5 Hz), 8.52 (br, 1H), 8.59 (d, 1H, J=4.9 Hz).

EXAMPLE 59

 

Synthesis of 4-[N-(4-Butylphenyl)-N-[2-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

4-(4-Butylanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (147 mg) and 2-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a dihydrochloride.

Yield: 59 mg (24%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 0.90 (t, 3H, J=7.4 Hz), 1.25-1.41 (m, 2H), 1.48-1.75 (m, 4H), 1.81 (d, 2H, J=11.7 Hz), 2.13 (t, 2H, J=11.2 Hz), 2.48 (t, 2H, J=7.5 Hz), 2.93 (d, 2H, J=11.2 Hz), 3.55 (s, 2H), 3.65-3.80 (m, 1H), 3.87 (s, 6H), 3.90 (s, 3H), 3.92 (s, 1H), 3.96 (s, 6H), 4.33 (s, 2H), 6.56 (s, 2H), 6.60 (d, 2H, J=8.5 Hz), 6.98 (d, 2H, J=8.5 Hz), 7.18 (d, 1H, J=4.9 Hz), 7.21 (s, 2H), 7.20-7.37 (m, 3H), 7.41 (br, 1H), 7.54 (s, 1H), 8.58 (d, 1H, J=4.9 Hz).

EXAMPLE 60

 

Synthesis of 4-[N-(4-Buthylphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(4-Butylanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (196 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (129 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as white powder after converting a free base to a trihydrochloride.

Yield: 20 mg (6%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 0.88 (t, 3H, J=7.3 Hz), 1.20-1.35 (m, 2H), 1.49-1.60 (m, 2H), 1.62-2.02 (m, 4H), 2.20 (br, 2H), 2.46 (t, 2H, J=7.3 Hz), 3.05 (br, 2H), 3.60 (br, 3H), 3.87 (s, 3H), 3.88 (s, 3H), 3.90 (s, 6H), 3.94 (s, 6H), 4.49 (s, 2H), 6.62 (d, 2H, J=8.3 Hz), 6.98 (d, 2H, J=8.3 Hz), 7.13 (s, 2H), 7.15-7.40 (m, 4H), 7.55 (br, 2H), 8.52 (d, 1H, J=4.9 Hz), 8.60 (br, 1H).

EXAMPLE 61

 

Synthesis of 4-[N-(4-Butylphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

4-(4-Butylanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (147 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a dihydrochloride.

Yield: 102 mg (42%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 0.90 (t, 3H, J=7.4 Hz), 1.30-1.36 (m, 2H), 1.48-1.56 (m, 2H), 1.76-1.89 (m, 4H), 2.19 (br, 2H), 2.48 (t, 2H, J=7.8 Hz), 2.97 (br, 2H), 3.58 (s, 2H), 3.86 (br, 1H), 3.88 (s, 3H), 3.58 (s, 2H), 3.86 (br, 1H), 3.88 (s, 3H), 3.90 (s, 3H), 3.95 (s, 6H), 4.54 (s, 2H), 6.68 (d, 2H, J=8.6 Hz), 6.72 (s, 2H), 7.00 (d, 2H, J=8.6 Hz), 7.20-7.27 (m, 2H), 7.23 (s, 2H), 7.32-7.40 (m, 2H), 7.44 (s, 1H), 7.62 (s, 1H), 8.59 (d, 1H, J=5.1 Hz).

EXAMPLE 62

 

Synthesis of 4-[N-(4-Butylphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-(4-Butylanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (147 mg) and 5-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a trihydrochloride.

Yield: 65 mg (21%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 0.90 (t, 3H, J=7.3 Hz), 1.32-1.36 (m, 2H), 1.50-1.54 (m, 2H), 1.70-1.95 (m, 4H), 2.17 (br, 2H), 2.49 (t, 2H, J=7.7 Hz), 2.96 (br, 2H), 3.58 (s, 2H), 3.75 (br, 1H), 3.89 (s, 3H), 3.90 (s, 3H), 3.94 (s, 6H), 3.96 (s, 6H), 4.50 (s, 2H), 6.68 (d, 2H, J=8.6 Hz), 7.00 (d, 2H, J=8.6 Hz), 7.20-7.22 (m, 3H), 7.23 (s, 2H), 7.58-7.66 (m, 3H), 8.59 (br, 1H), 8.60 (br, 1H).

EXAMPLE 63

 

Synthesis of 4-[N-(4-Butylphenyl)-N-[4-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride

4-(4-Butylanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (147 mg) and 4-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a dihydrochloride.

Yield: 82 mg (33%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 0.90 (t, 3H, J=7.3 Hz), 1.30-1.36 (m, 2H), 1.51-1.55 (m, 2H), 1.79-1.90 (m, 4H), 2.18 (br, 2H), 2.48 (t, 2H, J=7.7 Hz), 2.98 (d, 2H, J=10.7 Hz), 3.57 (s, 2H), 3.72-3.85 (m, 1H), 3.88 (s, 3H), 3.90 (s, 3H), 3.91 (s, 6H), 3.96 (s, 6H), 4.50 (s, 2H), 6.66 (d, 2H, J=8.8 Hz), 6.75 (s, 2H), 7.00 (d, 2H, J=8.8 Hz), 7.20 (d, 1H, J=4.9 Hz), 7.22 (s, 2H), 7.33 (d, 2H, J=8.2 Hz), 7.47 (d, 2H, J=8.2 Hz), 7.61 (s, 1H), 8.59 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 90 Synthesis of 1-(4-Pycolyl)-4-piperidone

4-piperidone hydrochloride monohydrate (922 mg) and 4-picolyl chloride hydrochloride (820 mg) were reacted in the same manner as described in Example 9 to give the title compound.

Yield: 870 mg (92%). ¹H-NMR (400 MHz, CDCl₃) δ: 2.46 (t, 4H, J=5.9 Hz), 2.74 (t, 4H, J=6.2 Hz), 3.61 (s, 2H), 7.29 (d, 2H, J=6.2 Hz), 8.55 (dd, 2H, J=6.2 Hz, 1.1 Hz).

PREPARATION EXAMPLE 91 Synthesis of 1-(4-Pycolyl)-4-(4-pycolylamino)piperidine Tetrahydrochloride

1-(4-pycolyl)-4-piperidone (870 mg) and 4-picolylamine (497 mg) were coupled in the same manner as described in Preparation Example 37. The title compound was obtained as pale brown powder after converting a free base to tetrahydrochloride.

Yield: 363 mg (19%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.37-1.51 (m, 2H), 1.82-1.90 (m, 2H), 2.04 (dt, 2H, J=11.6 Hz, 2.7 Hz), 2.44-2.55 (m, 1H), 2.76-2.82 (m, 2H), 3.47 (s, 2H), 3.82 (s, 2H), 7.23-7.26 (m, 4H), 8.50-8.53 (m, 4H).

PREPARATION EXAMPLE 92

Synthesis of 4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine

1-(tert-Butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[3-(3,4,5-trimethoxypheny)benzoyl]amino]piperidine Hydrochloride;

Yield: 125 g (74%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.23-1.35 (m, 2H), 1.46 (s, 9H), 1.96-2.06 (m, 2H), 2.83-2.96 (m, 2H), 3.27-3.38 (m, 1H), 3.74 (s, 9H), 3.94-4.12 (m, 2H), 6.58 (d, 2H, J=9.0 Hz), 6.77 (d, 2H, J=9.0 Hz).

PREPARATION EXAMPLE 93 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[3,4,5-trimethoxyphenyl)benzoylamino]piperidine

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (613 mg) and 3-(3,4,5-trimethoxyphenyl)benzoic acid (577 mg) were condensed in the same manner as described in Example 1 to give the title compound.

Yield: 416 mg (36%).

PREPARATION EXAMPLE 94 Synthesis of 4-[N-(4-Methoxyphenyl)-N-[3-(3,4,5-trimethoxypheny)benzoyl]amino]piperidine Hydrochloride

To a solution of

1-(tert-butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[3-(3,4,5-trimethoxypheny)benzoyl]amino]piperidine (416 mg) in ethyl acetate (5 mL) was added 4 M hydrogen chloride in ethyl acetate (5 mL). The mixture was stirred at room temperature for 4 hr, resulting precipitates were collected and washed with ethyl acetate on a funnel to give the title compound.

Yield: 315 mg (85%).

EXAMPLES 64 TO 66

 

These compounds were prepared by condensation of 4-[N-(4-methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzoyl]amino]piperidine hydrochloride with chloride derivatives obtained in Preparation Examples 3, 42 and 48. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Ex- am- NMR data (400 MHz, measured ple Structure Yield as free bases, CDCl₃) δ 64

68% 1.53-1.55(m, 2H), 1.89 (d, 2H, J=12.0 Hz), 2.23 (t, 2H, J=12.0 Hz), 2.91 (d, 2H, J=11.0 Hz), 3.51 (s, 2H), 3.70(s, 3H), 3.84(s, 3H), 3.87(s, 9H), 3.92(s, 6H), 4.78(br, 1H), 6.54(s, 2H), 6.72(d, 2H, J=8.5 Hz), 6.94(d, 2H, J=8.5 Hz), 7.13-7.20(m, 4H), 7.18(s, 2H), # 7.32(d, 1H, J=5.3 Hz), 7.45(s, 1H), 8.19(d, 1H, J=4.9 Hz). 65

52% 1.66-1.89(m, 4H), 2.05-2.17(m, 2H), 2.97(d, 2H, J=10.3 Hz), 3.43-3.60(m, 1H), 3.57(s, 2H), 3.86(s, 3H), 3.87(s, 6H), 3.87(s, 6H), 3.91(s, 6H), 4.42(s, 2H), 6.63(s, 2H), 6.72-6.79(m, 6H), 7.64(s, 1H), 7.78(br, 1H), 8.46 (d, 2H, J=1.6 Hz), 8.59(d, 1H, J=2.4 Hz), 8.68(d, 1H, J=2.2 Hz). 66

75% 1.42-1.58(m, 2H), 1.85-1.92(m, 2H), 2.14-2.23(m, 2H), 2.93-3.03 (m, 2H), 3.56(s, 2H), 3.70(s, 3H), 3.85(s, 3H), 3.87(s, 3H), 3.87(s, 6H), 3.90(s, 6H), 4.79(br, 1H), 6.54(s, 2H), 6.70(d, 2H, J=8.9 Hz), 6.74(s, 2H), 6.93(d, 2H, J=8.9 Hz), 7.17-7.23(m, 3H), 7.31-7.43(m, 5H).

The chemical names of the compounds of Examples 64 to 66 are:

EXAMPLE 64

 

4-[N-(4-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzoyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine EXAMPLE 65

 

4-[N-(4-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzoyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine EXAMPLE 66

 

4-[N-(4-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzoyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine PREPARATION EXAMPLE 95 Synthesis of 1-(tert-butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine:

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (2.21 g) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (2.12 g) were condensed in the same manner as described in Example 9 to give the title compound.

Yield: 3.76 g (93%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.40-1.64 (m, 2H), 1.44 (s, 9H), 1.82-1.91 (m, 2H), 2.71-2.84 (m, 2H), 3.62-3.73 (m, 1H), 3.74 (s, 3H), 3.89 (s, 3H), 3.94 (s, 6H), 4.10-4.30 (m, 2H), 4.40 (s, 2H), 6.76 (d, 2H, J=9.4 Hz), 6.79 (d, 2H, J=9.8 Hz), 7.14-7.19 (m, 3H), 7.56 (s, 1H), 8.55 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 96 Synthesis of 4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (3.76 g) was treated in the same manner as described in Preparation Example 94 to give the title compound.

Yield: 3.77 g (theoretical yield).

PREPARATION EXAMPLE 97 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine

4-(p-anisidino)-1-(tert-butoxycarbonyl)piperidine (613 mg) and 5-chloromethyl-3-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Preparation Example 9 to give pale yellow amorphous of the title compound.

Yield: 159 mg (14%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.44 (s, 9H), 1.50-1.65 (m, 2H), 1.83-1.91 (m, 2H), 2.70-2.84 (m, 2H), 3.53-3.62 (m, 1H), 3.73 (s, 3H), 3.89 (s, 3H), 3.91 (s, 6H), 4.10-4.29 (m, 2H), 4.41 (s, 2H), 6.66 (s, 2H), 6.76-6.84 (m, 4H), 7.70 (s, 1H), 8.49 (s, 1H), 8.63 (d, 1H, J=2.1 Hz).

PREPARATION EXAMPLE 98 Synthesis of 4-[N-(4-Methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine (159 mg) was treated in the same manner as described in Preparation Example 94 to give pale yellow powder of the title compound.

Yield: 142 mg (94%).

PREPARATION EXAMPLE 99 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (613 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (586 mg) was treated in the same manner as described in Example 9 to give pale yellow amorphous of the title compound.

Yield: 1.12 g (90%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.44 (s, 9H), 1.50-1.63 (m, 2H), 1.82-1.91 (m, 2H), 2.71-2.83 (m, 2H), 3.69 (tt, 1H, J=11.5 Hz, 3.5 Hz), 3.73 (s, 3H), 3.88 (s, 3H), 3.90 (s, 6H), 4.10-4.28 (m, 2H), 4.42 (s, 2H), 6.71 (s, 2H), 6.78 (s, 4H), 7.24-7.28 (m, 1H), 7.31-7.40 (m, 2H), 7.42 (s, 1H).

PREPARATION EXAMPLE 100 Synthesis of 4-[N-(4-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine Hydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine (1.12 g) was treated in the same manner as described in Preparation Example 94 to give pale yellow powder of the title compound.

Yield: 980 mg (99%).

EXAMPLES 67 TO 71

 

These compounds were obtained by the condensation of amines obtained in Preparation Examples 96, 98 and 100 with chloride derivatives obtained in Preparation Examples 42 and 48. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Ex- NMR data (400 MHz, mea- ample Structure Yield sured as free bases, CDCl₃) δ 67

62% 1.60-1.92(m, 4H), 2.08-2.22 (m, 2H), 2.92-3.06(m, 2H), 3.54-3.64(m, 3H), 3.73(s, 3H), 3.73(s, 3H), 3.89(s, 3H), 3.90(s, 3H), 3.93(s, 12H), 4.43(s, 2H), 6.70-6.81(m, 6H), 7.12-7.17(m, 3H), 7.56(s, 1H), 7.76(s, 1H), 8.49(d, 1H, J=1.8Hz), 8.53(d, 1H, J=5.1Hz), 8.70(s, 1H). 68

54% 1.65-1.79(m, 2H), 1.81-1.90 (m, 2H), 2.04-2.18(m, 2H), 2.94-3.06(m, 2H), 3.52-3.66 (m, 3H), 3.72(s, 3H), 3.89(s, 6H), 3.92(s, 6H), 3.93(s, 6H), 4.44(s, 2H), 6.70-6.80(m, 6H), 7.13-7.17(m, 3H), 7.24-7.50(m, 4H), 7.55(s, 1H), 8.53(d, 1H, J=4.9Hz). 69

52% 1.66-1.89(m, 4H), 2.05-2.17 (m, 2H), 2.97(d, 2H, J= 10.3Hz), 3.43-3.60(m, 1H), 3.57(s, 2H), 3.86(s, 3H), 3.87 (s, 6H), 3.91(s, 6H), 4.42(s, 2H), 6.63(s, 2H), 6.72-6.79 (m, 6H), 7.64(s, 1H), 7.78(br, 1H), 8.46(d, 2H, J=1.6Hz), 8.59(d, 1H, J=2.4Hz), 8.68 (d, 1H, J=2.2Hz). 70

69% 1.55-1.97(m, 4H), 2.06-2.21 (m, 2H), 2.92-3.07(m, 2H), 3.53-3.68(m, 3H), 3.72(s, 3H, 3.87(s, 3H), 3.89(s, 6H), 3.94(s, 3H), 4.46(s, 2H), 6.69(s, 2H), 6.73-6.82(m, 6H), 7.22-7.29(m, 1H), 7.32 (t,1H, J=7.4Hz), 7.36(d, 1H, J=7.8Hz), 7.41(s, 1H), 7.79 (br, 1H, 8.48(s, 1H), 8.71 (br, 1H). 71

75% 1.69-1.89(m, 4H), 2.06-2.15 (m, 2H), 2.96-3.04(m, 2H), 3.56-3.66(m, 1H), 3.57(s, 2H), 3.72(s, 3H), 3.87(s, 3H), 3.89(s, 9H), 3.92(s, 6H), 3.92(s, 6H), 4.46(s, 2H), 6.70(s, 2H), 6.71-6.79(m, 6H), 7.23-7.47(m, 8H).

The chemical names of the compounds of Examples 67 to 71 are:

EXAMPLE 67

 

4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 68

 

4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Dihydrochloride EXAMPLE 69

 

4-[N-(4-Methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 70

 

4-[N-(4-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Dihydrochloride EXAMPLE 71

 

4-[N-(4-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Hydrochloride PREPARATION EXAMPLE 101 Synthesis of 1-(tert-butoxycarbonyl)-4-(4-ethoxyphenylamino)piperidine:

1-(tert-butoxycarbonyl)-4-piperidinone (5.00 g) and p-phenetidine (3.28 g) was treated in the same manner as described in Preparation Example 37 to give brown powder of the title compound.

Yield: 7.00 g (91%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.21-1.31 (m, 2H), 1.37 (t, 3H, J=7.0 Hz), 1.46 (s, 9H), 1.97-2.05 (m, 2H), 2.84-2.95 (m, 2H), 3.28-3.37 (m, 1H), 3.96 (q, 2H, J=7.0 Hz), 3.99-4.10 (m, 2H), 6.57 (d, 2H, J=8.8 Hz), 6.77 (d, 2H, J=9.0 Hz).

PREPARATION EXAMPLE 102 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-ethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(4-ethoxyphenyl)amino]piperidine (641 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 1.08 g (94%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.36 (t, 3H, J=7.9 Hz), 1.44 (s, 9H), 1.49-1.58 (m, 2H), 1.82-1.92 (m, 2H), 2.70-2.85 (m, 2H), 3.62-3.72 (m, 1H), 3.89 (s, 3H), 3.94 (s, 6H), 4.12-4.29 (m, 2H), 4.39 (s, 2H), 6.75 (d, 2H, J=9.2 Hz), 6.78 (d, 2H, J=9.6 Hz), 7.14-7.18 (m, 3H), 7.55 (s, 1H), 8.54 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 103 Synthesis of 4-[N-(4-Ethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-ethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (1.08 g) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 1.01 g (98%).

PREPARATION EXAMPLE 104 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-ethoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(4-ethoxyphenyl)amino]piperidine (641 mg) and 5-chloromethyl-3-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 452 mg (39%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.36 (t, 3H, J=6.8 Hz), 1.44 (s, 9H), 1.50-1.60 (m, 2H), 1.82-1.90 (m, 1H), 2.68-2.82 (m, 2H), 3.52-3.61 (m, 1H), 3.88 (s, 3H), 3.90 (s, 6H), 3.94 (q, 2H, J=7.0 Hz), 4.10-4.25 (m, 2H), 4.40 (s, 2H), 6.66 (s, 2H), 6.77 (d, 2H, J=9.2 Hz), 6.81 (d, 2H, J=9.2 Hz), 7.67 (s, 1H), 8.49 (d, 1H, J=2.0 Hz), 8.62 (d, 1H, J=2.1 Hz).

PREPARATION EXAMPLE 105 Synthesis of 4-[N-(4-Ethoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-ethoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine (452 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 380 mg (88%).

PREPARATION EXAMPLE 106 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-ethoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(4-ethoxyphenyl)amino]piperidine (641 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (586 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 1.06 g (92%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.36 (t, 3H, J=7.0 Hz), 1.44 (s, 9H), 1.53-1.59 (m, 2H), 1.83-1.91 (m, 2H), 2.70-2.83 (m, 2H), 3.64-3.73 (m, 1H), 3.88 (s, 3H), 3.90 (s, 6H), 3.94 (q, 2H, J=7.0 Hz), 4.10-4.29 (m, 2H), 4.41 (s, 2H), 6.71 (s, 2H), 6.76 (s, 4H), 7.26 (d, 1H, J=7.9 Hz), 7.33 (dd, 1H, J=7.4 Hz, 7.4 Hz), 7.38 (d, 1H, J=7.6 Hz), 7.42 (s, 1H).

PREPARATION EXAMPLE 107 Synthesis of 4-[N-(4-Ethoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine Hydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-ethoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine (1.06 g) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 913 mg (97%).

EXAMPLES 72 TO 79

 

These compounds were obtained by the condensation of amines obtained in Preparation Examples 103, 105 and 107 with chloride derivatives obtained in Preparation Examples 3, 42 and 48. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Ex- am- NMR data (400 MHz, measured ple Structure Yield as free bases, CDCl₃) δ 72

49% 1.36(t, 3H, J=7.1 Hz), 1.68-1.94 (m, 4H), 2.10-2.24(m, 2H), 2.93-3.04(m, 2H), 3.54-3.65(m, 3H), 3.89(s, 3H), 3.90(s, 3H), 3.93(s, 6H), 3.96(s, 6H), 4.45(s, 2H), 6.72(d, 2H, J=9.2 Hz), 6.78 (d, 2H, J=9.3 Hz), 7.15(s, 2H), 7.17(d, 1H, J=6.1 Hz), 7.20(dd, # 1H, J=4.9 Hz, 1.0 Hz), 7.23(s, 2H), 7.57(s, 1H), 7.61(br, 1H), 8.54(d, 1H, J=5.2 Hz), 8.59(d, 1H, J=4.9 Hz). 73

63% 1.36(t, 3H, J=7.0 Hz), 1.56-1.74 (m, 2H), 1.80-1.90(m, 2H), 2.07-2.19(m, 2H), 2.92-3.02(m, 2H), 3.58(s, 2H), 3.88-3.95(m, 2H), 3.89(s, 3H), 3.93(s, 12H), 4.43(s, 2H), 6.69-6.79(m, 6H), 7.12-7.17(m, 3H), 7.55(s, 1H), 7.76(s, 1H), 8.49(d, 1H, J=1.8 # Hz), 8.53(d, 1H, J=5.1 Hz), 8.69 (s, 1H). 74

65% 1.36(t, 3H, J=7.0 Hz), 1.58-1.78 (m, 2H), 1.80-1.89(m, 2H), 2.04-2.16(m, 2H), 2.95-3.05(m, 2H), 3.52-3.66(m, 1H), 3.57(s, 1H), 3.85-3.97(m, 2H), 3.89(s, 6H), 3.92(s, 6H), 3.93(s, 6H), 4.44(s, 2H), 6.67-6.80(m, 6H), 7.13-7.18(m, 3H),7.25-7.31(m, # 1H), 7.37(dd, 1H, J=7.6 Hz, 7.6 Hz), 7.41-7.48(m, 2H), 7.55(s, 1H), 8.53(d, 1H, J=4.9 Hz). 75

42% 1.36(t, 3H, J=7.0 Hz), 1.74-2.34 (m, 6H), 2.96-3.10(m, 2H), 3.47-3.73(m, 3H), 3.87-3.98(m, 2H), 3.88(s, 3H), 3.90(s, 9H), 3.97(s, 6H), 4.44(s, 2H), 6.65(s, 2H), 6.74-6.82(m, 4H), 7.18-7.32 (m, 4H), 7.67(s, 1H), 8.49(d, 1H, J=1.6 Hz), 8.57-8.65(m, 2H). 76

43% 1.36(t, 3H, J=6.8 Hz), 1.63-1.96 (m, 4H), 2.00-2.26(m, 2H), 2.92-3.03(m, 2H), 3.44-3.66(m, 3H), 3.86-3.96(m, 2H), 3.88(s, 3H), 3.89(s, 6H), 3.90(s, 3H), 3.93(s, 6H), 4.44(s, 2H), 6.65(s, 2H), 6.72-6.80(m, 6H), 7.67(s, 1H), 7.77(br, 1H), 8.47-8.53(m, 2H), 8.62(d, 1H, J=1.9 Hz), 8.70 # (s, 1H). 77

82% 1.35(t, 3H, J=6.8 Hz), 1.70-1.82 (m, 2H), 1.84-1.92(m, 2H), 2.10-2.19(m, 2H), 2.92-3.00(m, 2H), 3.52-3.65(m, 3H), 3.88(s, 3H), 3.89(s, 6H), 3.90(s, 3H), 3.93(q, 2H, J=7.1 Hz), 3.96(s, 6H), 4.47(s, 2H), 6.70(s, 2H), 6.73(d, 2H, J=9.3 Hz), 6.77(d, # 2H, J=9.3 Hz), 7.18-7.28(m, 4H), 7.33(dd, 1H, J=7.3 Hz, 7.3 Hz), 7.37(d, 1H, J=7.6 Hz), 7.43(s, 1H), 7.59(s, 1H), 8.58(d, 1H, J=4.9 Hz). 78

61% 1.35(t, 3H, J=6.9 Hz), 1.58-1.80 (m, 2H), 1.82-1.91(m, 2H), 2.09-2.18(m, 2H), 2.93-3.20(m, 2H), 3.56-3.65(m, 1H), 3.58(s, 2H), 3.87(s, 3H), 3.89(s, 6H), 3.89(s, 3H), 3.91-3.94(m, 2H), 3.93(s, 6H), 4.45(s, 2H), 6.69(s, 2H), 6.71-6.78(m, 6H), 7.23-7.28 # (m, 1H), 7.32(t, 1H, J=7.5 Hz), 7.36(d, 1H, J=7.6 Hz), 7.42(s, 1H), 7.77(s, 1H), 8.49(d, 1H, J=1.8 Hz), 8.69(d, 1H, J=1.8 Hz). 79

73% 1.35(t, 3H, J=6.8 Hz), 1.68-1.80 (m, 2H), 1.81-1.89(m, 2H), 2.06-2.14(m, 2H), 2.96-3.03(m, 2H), 3.57(s, 2H), 3.57-3.65(m, 1H), 3.87(s, 3H), 3.89(s, 9H), 3.91-3.96(m, 2H), 3.92(s, 6H), 4.46(s, 2H), 6.69-6.79(m, 9H), 7.23-7.47(m, 7H).

The chemical names of the compounds of Examples 72 to 79 are:

EXAMPLE 72

 

4-[N-(4-Ethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 73

 

4-[N-(4-Ethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 74

 

4-[N-(4-Ethoxyphenyl)-N- [[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Dihydrochloride EXAMPLE 75

 

4-[N-(4-Ethoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 76

 

4-[N-(4-Ethoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 77

 

4-[N-(4-Ethoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride EXAMPLE 78

 

4-[N-(4-Ethoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Dihydrochloride EXAMPLE 79

 

4-[N-(4-Ethoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Hydrochloride PREPARATION EXAMPLE 108 Synthesis of 1-(tert-butpxycarbonyl)-4-4-butoxyphenylamino)piperidine:

1-(tert-butoxycarbonyl)-4-piperidone (5.00 g) and 4-butoxyaniline (3.95 g) was treated in the same manner as described in Preparation Example 37 to give brown powder of the title compound.

Yield: 6.91 g (83%). ¹H-NMR (400 MHz, CDCl₃) δ: 0.96 (t, 3H, J=7.2 Hz), 1.23-1.35 (m, 2H), 1.42-1.53 (m, 2H), 1.46 (s, 9H), 1.68-1.76 (m, 2H), 1.97-2.05 (m, 2H), 2.84-2.95 (m, 2H), 3.28-3.37 (m, 1H), 3.88 (t, 2H, J=6.6 Hz), 3.96-4.12 (m, 2H), 6.57 (d, 2H, J=9.0 Hz), 6.77 (d, 2H, J=8.8 Hz).

PREPARATION EXAMPLE 109 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-butoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(4-butoxyphenyl)amino]piperidine (696 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 980 mg (81%). ¹H-NMR (400 MHz, CDCl₃) δ: 0.95 (t, 3H, J=7.4 Hz), 1.40-1.50 (m, 2H), 1.44 (s, 9H), 1.67-1.76 (m, 2H), 1.82-1.90 (m, 2H), 1.82-1.90 (m, 2H), 2.70-2.82 (m, 2H), 3.61-3.71 (m, 1H), 3.84-3.90 (m, 5H), 3.94 (s, 6H), 4.10-4.28 (m, 2H), 4.39 (s, 2H), 6.74 (d, 2H, J=9.4 Hz), 6.78 (d, 2H, J=9.4 Hz), 7.14-7.18 (m, 3H), 7.56 (s, 1H), 8.54 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 110 Synthesis of 4-[N-(4-Butoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-butoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (980 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 926 mg (99%).

PREPARATION EXAMPLE 111 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-butoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(4-butoxyphenyl)amino]piperidine (697 mg) and 5-chloromethyl-3-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 485 mg (40%). ¹H-NMR (400 MHz, CDCl₃) δ: 0.95 (t, 3H, J=7.4 Hz), 1.40-1.57 (m, 2H), 1.44 (s, 9H), 1.67-1.75 (m, 2H), 1.82-1.90 (m, 2H), 2.69-2.81 (m, 2H), 3.51-3.60 (m, 1H), 3.87 (q, 2H, J=6.6 Hz), 3.88 (s, 3H), 3.90 (s, 6H), 4.06-4.23 (m, 2H), 4.39 (s, 2H), 6.66 (s, 2H), 6.77 (d, 2H, J=9.2 Hz), 6.81 (d, 2H, J=9.2 Hz), 6.81 (d, 2H, J=9.4 Hz), 7.67 (s, 1H), 8.49 (d, 1H, J=1.8 Hz), 8.62 (d, 1H, J=2.2 Hz).

PREPARATION EXAMPLE 112 Synthesis of 4-[N-(4-Butoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-butoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine (485 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 456 mg (98%).

PREPARATION EXAMPLE 113 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-butoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(4-butoxyphenyl)amino]piperidine (697 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (586 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 1.17 g (97%). ¹H-NMR (400 MHz, CDCl₃) δ: 0.95 (t, 3H, J=7.3 Hz), 1.40-1.61 (m, 4H), 1.44 (s, 9H), 1.67-1.75 (m, 2H), 1.83-1.90 (m, 2H), 2.70-2.83 (m, 2H), 3.63-3.72 (m, 2H), 3.87 (q, 2H, J=6.6 Hz), 3.88 (s, 3H), 3.90 (s, 6H), 4.09-4.28 (m, 2H), 4.41 (s, 2H), 6.70 (s, 2H), 6.76 (s, 4H), 7.26 (d, 2H, J=8.0 Hz), 7.33 (t, 1H, J=7.6 Hz), 7.38 (d, 1H, J=7.3 Hz), 7.42 (s, 1H).

PREPARATION EXAMPLE 114 Synthesis of 4-[N-(4-Butoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine Hydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-butoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine (1.17 g) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 1.02 g (98%).

EXAMPLE 80 TO 87

 

These compounds were obtained by the condensation of amines obtained in Preparation Examples 110, 112 and 114 with chloride derivatives obtained in Preparation Examples 3, 42 and 48. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Ex- am- NMR data (400 MHz, measured ple Structure Yield as free bases, CDCl₃) δ 80

63% 0.95(t, 3H, J=7.3 Hz), 1.40-1.51 (m, 2H), 1.66-1.79(m, 2H), 1.83-1.92(m, 2H), 2.10-2.21(m, 2H), 2.92-3.02(m, 2H), 3.53-3.63 (m, 3H), 3.84-3.90(m, 2H), 3.89 (s, 3H), 3.93(s, 6H), 3.96(s, 6H), 6.72(d, 2H, J=9.3 Hz), 6.77(d, 2H, J=9.3 Hz), 7.15(s, 2H), 7.17 # (d, 1H, J=5.1 Hz), 7.20(d, 1H, J=6.1 Hz), 7.22(s, 2H), 7.57(s, 1H), 7.59(s, 1H), 8.54(d, 1H, J=4.9 Hz), 8.59(d, 1H, J=5.1 Hz). 81

44% 0.95(t, 3H), J=7.4 Hz), 1.42-1.51 (m, 2H), 1.67-1.76(m, 4H), 1.80-1.91(m, 2H), 2.08-2.20(m, 2H), 2.92-3.03(m, 2H), 3.84-3.96 (m, 3H), 3.89(s, 3H), 3.90(s, 3H), 3.93(s, 12H), 4.43(s, 2H), 6.69-6.79(m, 6H), 7.14(s, 2H), 7.16(d, 1H, J=5.2 Hz), 7.55(s, # 1H), 7.76(s, 1H), 8.49(d, 1H, J=1.8 Hz), 8.53(d, 1H, J=5.0 Hz), 8.69(s, 1H). 82

53% 0.95(t, 3H, J=7.2 Hz), 1.40-1.51 (m, 2H), 1.65-1.78(m, 4H), 1.81- 1.89(m,2H), 2.05-2.18(m, 2H), 3.05-3.06(m, 2H), 3.54-3.65(m, 3H), 3.84-3.96(m, 20H), 4.44(s, 2H), 6.70(d, 2H, J=9.2 Hz), 6.74- 6.80(m, 4H), 7.11-7.19(m, 3H), 7.22-7.32(m, 1H), 7.34-7.50(m, # 3H), 7.55(s, 1H), 8.53(d, 1H, J=5.1 Hz). 83

42% 0.95(t, 3H, 7.4 Hz), 1.40-1.51(m, 2H), 1.67-1.86(m, 6H), 2.03-2.30 (m, 2H), 2.92-3.06(m, 2H), 3.46- 3.56(m, 1H), 3.60(s, 2H), 3.84- 3.91(m, 2H), 3.88(s, 3H), 3.89 (s, 6H), 3.90(s, 3H), 3.96(s, 6H), 4.44(s, 2H), 6.65(s, 2H), 6.74- 6.81(m, 4H), 7.20(d, 1H, J=4.9 Hz), 7.25(s, 2H), 7.67(br, 2H), # 8.50(d, 1H, J=1.6 Hz), 8.60(d, 1H, J=5.6 Hz). 84

36% 0.95(t, 3H, J=7.4 Hz), 1.40-1.51 (m, 2H), 1.66-1.79(m, 4H), 1.82-1.92(m, 2H), 2.00-2.22(m, 2H), 2.83-3.06(m, 2H), 3.44-3.67 (m, 3H), 3.82-3.97(m, 2H), 3.88 (s, 3H), 3.89(s, 6H), 3.90(s, 3H), 3.93(s, 6H), 4.44(s, 2H), 6.65(s, 2H), 6.72-6.80(m, 6H), 7.67(s, # 1H), 7.76(br, 1H), 8.47-8.53(m, 2H), 8.62(d, 1H, J=2.2 Hz), 8.70 (s, 1H). 85

72% 0.95(t, 3H, J=7.3 Hz), 1.40-1.51 (m, 2H), 1.66-1.82(m, 4H), 1.84-1.92(m, 2H), 2.10-2.20(m, 2H), 2.92-3.00(m, 2H), 3.53-3.66 (m, 3H), 3.83-3.92(m, 2H), 3.88 (s, 3H), 3.89(s, 6H), 3.90(s, 3H), 3.96(s, 6H), 4.47(s, 2H), 6.67(s, 2H), 6.73(d, 2H, J=9.2 Hz), 6.77 # (d, 2H, J=9.5 Hz), 7.18-7.29(m, 4H), 7.33(dd, 1H, J=7.3 Hz, 7.3 Hz), 7.37(d, 1H, J=7.6 Hz), 7.43 (s, 1H), 7.60(s, 1H), 8.58(d, 1H, J=4.9 Hz). 86

24% 0.94(t, 3H, J=7.4 Hz), 1.41-1.51 (m, 2H), 1.61-1.80(m, 4H), 1.82-1.92(m, 2H), 2.08-2.19(m, 2H), 2.92-3.02(m, 2H), 3.55-3.65 (m, 1H), 3.57(s, 2H), 3.84-3.91 (m, 2H), 3.87(s, 3H), 3.88(s, 6H), 3.89(s, 3H), 3.93(s, 6H), 4.45(s, 2H), 6.69(s, 2H), 6.71-6.78(m, # 4H), 6.75(s, 2H), 7.23-7.28(m, 1H), 7.32(t, 1H, J=7.4 Hz), 7.36 (d, 1H, J=7.6 Hz), 7.42(s, 1H), 7.77(s, 1H), 8.49(d, 1H, J=1.6 Hz), 8.69(s, 1H). 87

78% 0.94(t, 3H, J=7.3 Hz), 1.40-1.50 (m, 2H), 1.66-1.88(m, 4H), 1.82-1.89(m, 2H), 2.04-2.16(m, 2H), 2.96-3.03(m, 2H), 3.55-3.65 (m, 3H), 3.83-3.90(m, 2H), 3.87 (s, 3H), 3.89(s, 9H), 3.92(s, 6H), 4.46(s, 2H), 6.69-6.79(m, 9H), 7.23-7.48(m, 7H).

The chemical names of the compounds of Examples 80 to 87 are:

EXAMPLE 80

 

4-[N-(4-Butoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 81

 

4-[N-(4-Butoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 82

 

4-[N-(4-Butoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Dihydrochloride EXAMPLE 83

 

4-[N-(4-Butoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 84

 

4-[N-(4-Butoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 85

 

4-[N-(4-Butoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride EXAMPLE 86

 

4-[N-(4-Butoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Dihydrochloride EXAMPLE 87

 

4-[N-(4-Butoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Hydrochloride PREPARATION EXAMPLE 115 Synthesis of 4-(m-Anisidino)-1-(tert-butoxycarbonyl)piperidine

1-(tert-Butoxycarbonyl)-4-piperidone (4.78 g) and m-anisidine (2.96 g) were condensed in the same manner as described in Preparation Example 37 to give the title compound.

Yield: 4.83 g (66%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.20-1.39 (m, 2H), 1.44 (s, 9H), 1.99-2.05 (m, 2H), 2.89 (dt, 2H, J=13.5 Hz, 2.2 Hz), 3.33-3.44 (m, 1H), 3.75 (s, 3H), 3.96-4.07 (m, 2H), 6.14 (t, 1H, J=2.2 Hz), 6.18-6.29 (m, 2H), 7.05 (t, 1H, J=8.1 Hz).

PREPARATION EXAMPLE 116 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(3-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

4-(m-Anisidino)-1-(tert-butoxycarbonyl)piperidine (613 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 789 mg (70%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.50-1.67 (m, 2H), 1.82-1.91 (m, 2H), 2.74-2.87 (m, 2H), 3.74 (s, 3H), 3.88-3.98 (m, 1H), 3.89 (s, 3H), 3.94 (s, 6H), 4.14-4.32 (m, 2H), 4.48 (s, 2H), 6.28 (dd, 1H, J=2.2 Hz, 2.2 Hz), 6.31-6.37 (m, 2H), 7.10-7.15 (m, 2H), 7.16 (s, 2H), 7.55 (s, 1H), 8.56 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 117 Synthesis of 4-[N-(3-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(3-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (789 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 710 mg (95%).

PREPARATION EXAMPLE 118 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(3-methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine

4-(m-Anisidino)-1-(tert-butoxycarbonyl)piperidine (613 mg) and 5-chloromethyl-3-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 396 mg (35%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.54-1.66 (m, 2H), 1.81-1.91 (m, 2H), 2.73-2.87 (m, 2H), 3.74 (s, 3H), 3.87-3.93 (m, 1H), 3.88 (s, 3H), 3.90 (s, 6H), 4.14-4.29 (m, 2H), 4.51 (s, 2H), 6.30-6.35 (m, 2H), 6.38 (d, 1H, J=7.2 Hz), 6.68 (s, 2H), 7.12 (dd, 1H, J=8.8 Hz, 8.88 Hz), 7.66 (s, 1H), 8.49 (d, 1H, J=2.0 Hz), 8.66 (d, 1H, J=2.2 Hz).

PREPARATION EXAMPLE 119 Synthesis of 4-[N-(3-Methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(3-methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine (396 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 348 mg (92%).

PREPARATION EXAMPLE 120 Synthesis of 1-(tert-Butoxycarbonyl)4-[N-(3-methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine

4-(m-Anisidino)-1-(tert-butoxycarbonyl)piperidine (613 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (586 mg) was treated in the same manner as described in Preparation Example 9 to give light yellow amorphous of the title compound.

Yield: 1.01 g (90%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.44 (s, 9H), 1.56-1.67 (m, 2H), 1.83-1.91 (m, 2H), 2.72-2.86 (m, 2H), 3.73 (s, 3H), 3.85-3.98 (m, 1H), 3.88 (s, 3H), 3.90 (s, 6H), 4.12-4.30 (m, 2H), 4.50 (s, 2H), 6.27-6.34 (m, 2H), 6.38 (dd, 1H, J=8.2 Hz, 2.4 Hz), 6.72 (s, 2H), 7.10 (dd, 1H, J=8.2 Hz, 8.2 Hz), 7.21-7.27 (m, 1H), 7.32-7.43 (m, 3H).

PREPARATION EXAMPLE 121 Synthesis of 4-[N-(3-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine Hydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(3-methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine (1.01 g) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 820 mg (92%).

EXAMPLES 88 TO 95

 

These compounds were obtained by the condensation of amines obtained in Preparation Examples 117, 119 and 121 with chloride derivatives obtained in Preparation Examples 3, 42 and 48. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Ex- am- NMR data (400 MHz, measured ple Structure Yield as free bases, CDCl₃) δ 88

63% 1.70-1.82(m, 2H), 1.83-1.90(m, 2H), 2.14-2.23(m, 2H), 2.94-3.01 (m, 2H), 3.57(s, 2H), 3.73(s, 3H), 3.76-3.88(m, 1H), 3.89(s, 3H), 3.90(s, 3H), 3.93(s, 6H), 3.96(s, 6H), 4.53(s, 2H), 6.26-6.35(m, 3H), 7.11(dd, 1H, J=8.3 Hz, 8.3 Hz), 7.12-7.14(m, 1H), 7.15(s, # 2H), 7.20(d, 1H, J=5.1 Hz), 7.22 (s, 2H), 7.55(s, 1H), 7.58(s, 1H), 8.55(d, 1H, J=4.9 Hz), 8.59(d, 1H, J=4.9 Hz). 89

72% 1.67-1.90(m, 4H), 2.13-2.22(m, 2H), 2.94-3.04(m, 2H), 3.59(s, 2H), 3.74(s, 3H), 3.77-3.87(m, 1H), 3.89(s, 3H), 3.89(s, 3H), 3.92(s, 6H), 3.93(s, 6H), 4.52(s, 2H), 6.27(dd, 1H, J=2.4 Hz, 2.4 Hz), 6.29-6.34(m, 2H), 6.75(s, 2H), 7.08-7.17(m, 4H), 7.54(s, # 1H), 7.75(s, 1H), 8.50(d, 1H, J=1.8 Hz), 8.54(d, 1H, J=5.1 Hz), 8.69(d, 1H, J=2.0 Hz). 90

60% 1.68-1.90(m, 4H), 2.09-2.19(m, 2H), 2.97-3.06(m, 2H), 3.58(s, 2H), 3.73(s, 3H), 3.76-3.87(m, 1H), 3.89(s, 6H), 3.92(s, 6H), 3.92(s, 6H), 4.52(s, 2H), 6.25-6.35(m, 3H), 6.76(s, 2H), 6.78-7.17(m, 4H), 7.25-7.32(m, 1H), 7.37(dd, 1H, J=7.4 Hz, 7.4 Hz), 7.41-7.47(m, 2H), 7.54(s, # 1H), 8.54(d, 1H, J=5.1 Hz). 91

50% 1.80-1.93(m, 4H), 2.13-2.32(m, 2H), 2.87-3.10(m, 2H), 3.60(s, 1H), 3.69-3.85(m, 1H), 3.73(s, 3H), 3.88(s, 3H), 3.89(s, 6H), 3.90(s, 3H), 3.96(s, 6H), 4.57(s, 2H), 6.29-6.34(m, 2H), 6.37(dd, 1H, J=8.2 Hz, 8.1 Hz), 6.67(s, 2H), 7.11(dd, 1H, J=8.6 Hz, 8.6 Hz), 7.20-7.28(m, 3H), 7.58-7.72 # (m, 1H), 7.68(s, 1H), 8.50(d, 1H, J=1.8 Hz), 8.60(d, 1H, J=4.7 Hz), 8.65(d, 1H, J=2.0 Hz). 92

35% 1.70-1.90(m, 4H), 2.12-2.25(m, 2H), 2.95-3.03(m, 2H), 3.59(s, 2H), 3.72-3.97(m, 1H), 3.73(s, 3H), 3.88(s, 3H), 3.89(s, 6H), 3.90(s, 3H), 3.93(s, 6H), 4.54(s, 2H), 6.25-6.38(m, 2H), 6.36(d, 1H, J=8.4 Hz, 8.4 Hz), 6.67(s, 2H), 6.75(s, 2H), 7.11(dd, 1H, J=8.4 Hz), 7.66(s, 1H), 8.49(s, # 1H), 8.50(d, 1H, J=1.8 Hz), 8.64 (d, 1H, J=2.0 Hz), 8.70(d, 1H, J=1.9 Hz). 93

86% 1.73-1.93(m, 4H), 2.13-2.23(m, 2H), 2.94-3.02(m, 2H), 3.57(s, 2H), 3.73(s, 3H), 3.77-3.87(m, 1H), 3.88(s, 3H), 3.88(s, 6H), 3.90(s, 3H), 3.96(s, 6H), 4.56 (s, 2H), 6.27(dd, 1H, J=8.0 Hz, 2.2 Hz), 6.31(dd, 1H, J=2.2 Hz, 2.2 Hz), 6.36(dd, 1H, J=8.2 Hz, 2.2 # Hz), 6.71(s, 2H), 7.09(dd, 1H, J=8.1 Hz, 8.1 Mz), 7.18-7.28(m, 4H), 7.34(dd, 1H, J=7.4 Hz, 7.4 Hz), 7.38(d, 1H, J=7.6 Hz), 7.42 (s, 1H), 7.59(s, 1H), 8.59(d, 1H, J=4.9 Hz). 94

56% 1.72-1.92(m, 4H), 2.10-2.23(m, 2H), 2.92-3.60(m, 2H), 3.59(s, 2H), 3.72(s, 3H), 3.77-3.89(m, 1H), 3.87(s, 3H), 3.88(s, 6H), 3.93(s, 6H), 4.55(s, 2H), 6.27 (dd, 1H, J=8.0 Hz, 2.2 Hz), 6.31 (dd, 1H, J=2.1 Hz, 2.1 Hz), 6.36 (dd, 1H, J=8.4 Hz, 2.4 Hz), 6.70 (s, 2H), 6.75(s, 2H), 7.09(dd, 1H, # J=8.2 Hz, 8.2 Hz), 7.22(d, 1H, J=7.4 Hz), 7.33(dd, 1H, J=7.4 Hz, 7.4 Hz), 7.38(d, 1H, J=7.8 Hz), 7.40(s, 1H), 7.77(s, 1H), 8.50(d, 1H, J=1.8 Hz), 8.69(d, 1H, J=1.8 Hz). 95

77% 1.66-1.89(m, 4H), 2.08-2.18(m, 2H), 2.95-3.05(m, 2H), 3.58(s, 2H), 3.72(s, 3H), 3.75-3.84(m, 1H), 3.87(s, 3H), 3.88(s, 6H), 3.89(s, 3H), 3.92(s, 6H), 4.55(s, 2H), 6.26(dd, 1H, J=8.0 Hz, 2.2 Hz), 6.30(dd, 1H, J=2.2 Hz, 2.2 Hz), 6.36(dd, 1H, J=8.3 Hz, 2.2 # Hz), 6.70(s, 2H), 6.76(s, 2H), 7.08(dd, 1H, J=8.3 Hz, 8.3 Hz), 7.22(d, 1H, J=7.3 Hz), 7.27-7.47 (m, 7H).

The chemical names of the compounds of Examples 88 to 95 are:

EXAMPLE 88

 

4-[N-(3-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 89

 

4-[N-(3-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 90

 

4-[N-(3-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Dihydrochloride EXAMPLE 91

 

4-[N-(3-Methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 92

 

4-[N-(3-Methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 93

 

4-[N-(3-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride EXAMPLE 94

 

4-[N-(3-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Dihydrochloride EXAMPLE 95

 

4-[N-(3-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxypheny)benzyl]piperidine Hydrochloride PREPARATION EXAMPLE 122 Synthesis of 4-(o-anisidino)-1-(tert-butoxycarbonyl)piperidine:

1-(tert-Butoxycarbonyl)-4-piperidone (4.78 g) and o-anisidine (2.96 g) were condensed in the same manner as described in Preparation Example 37 to give the title compound.

Yield: 2.61 g (36%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.31-1.41 (m, 2H), 1.47 (s, 9H), 2.00-2.08 (m, 2H), 2.90-3.01 (m, 2H), 3.38-3.47 (m, 1H), 3.83 (s, 3H), 4.00-4.21 (m, 2H), 6.60-6.69 (m, 2H), 6.76-6.89 (m, 2H).

PREPARATION EXAMPLE 123 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(2-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

4-(o-Anisidino)-1-(tert-butoxycarbonyl)piperidine (613 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 763 mg (68%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.41-1.58 (m, 2H), 1.44 (s, 9H), 1.81-1.91 (m, 2H), 2.62-2.78 (m, 2H), 3.29 (tt, 1H, J=7.6 Hz, 3.7 Hz), 3.86 (s, 3H), 3.89 (s, 3H), 3.95 (s, 6H), 4.06-4.16 (m, 2H), 4.37 (s, 2H), 6.80 (ddd, 1H, J=7.6 Hz, 7.6 Hz, 1.2 Hz), 6.87 (dd, 1H, J=8.5 Hz, 1.0 Hz), 7.00-7.06 (m, 2H), 7.14 (s, 2H), 7.20 (dd, 1H, J=4.9 Hz, 1.0 Hz), 7.61 (s, 1H), 8.49 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 124 Synthesis of 4-[N-(2-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(2-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (763 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 701 mg (97%).

PREPARATION EXAMPLE 125 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(2-methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine

4-(o-Anisidino)-1-(tert-butoxycarbonyl)piperidine (613 mg) and 5-chloromethyl-3-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 353 mg (31%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.44 (s, 9H), 1.46-1.53 (m, 2H), 1.82-1.91 (m, 2H), 2.62-2.78 (m, 2H), 3.24-3.33 (m, 1H), 3.83 (s, 3H), 3.89 (s, 3H), 3.91 (s, 6H), 4.03-4.16 (m, 2H), 4.37 (s, 2H), 6.64 (s, 2H), 6.79 (ddd, 1H, J=7.6 Hz, 7.6 Hz, 1.2 Hz), 6.84 (dd, 1H, J=7.0 Hz, 1.2 Hz), 6.97-7.06 (m, 2H), 7.68 (dd, 1H, J=1.3 Hz, 1.3 Hz), 8.49 (d, 1H, J=2.0 Hz), 8.56 (d, 1H, J=2.2 Hz).

PREPARATION EXAMPLE 126 Synthesis of 4-[N-(2-Methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(2-methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine (353 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 312 mg (93%).

PREPARATION EXAMPLE 127 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(2-methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine

4-(o-Anisidino)-1-(tert-butoxycarbonyl)piperidine (613 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (586 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 1.12 g (100%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.43 (s, 9H), 1.46-1.57 (m, 2H), 1.81-1.90 (m, 2H), 2.62-2.76 (m, 2H), 3.31 (tt, 1H, J=11.1 Hz, 3.3 Hz), 3.84 (s, 3H), 3.88 (s, 3H), 3.91 (s, 6H), 4.00-4.16 (m, 2H), 4.36 (s, 2H), 6.67 (s, 2H), 6.78 (t, 1H, J=7.3 Hz), 6.85 (d, 1H, J=7.9 Hz), 6.96-7.03 (m, 2H), 7.24-7.34 (m, 3H), 7.43 (s, 1H).

PREPARATION EXAMPLE 128 Synthesis of 4-[N-(2-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine Hydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(2-methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine (1.12 g) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 987 mg (99%).

EXAMPLES 96 TO 101

 

These compounds were obtained by the condensation of amines obtained in Preparation Examples 124, 126 and 128 with chloride derivatives obtained in Preparation Examples 3 and 48. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Ex- am- NMR data (400 MHz, measured as ple Structure Yield free bases, CDCl₃) δ  96

73% 1.62-1.74(m, 2H), 1.82-1.90(m, 2H), 1.98-2.08(m, 2H), 2.86-2.94 (m, 2H), 3.13-3.22(m, 1H), 3.52 (s, 2H), 3.85(s, 3H), 3.89(s, 3H), 3.90(s, 3H), 3.94(s, 6H), 3.96(s, 6H), 4.40(s, 2H), 6.80(ddd, 1H, J=7.6 Hz, 7.6 Hz, 1.2 Hz), 6.86 (dd, 1H, J=8.1 Hz, 1.2 Hz), 6.98-7.05(m, 1H), 7.14(s, 2H), # 7.18(dd, 1H, J=4.9 Hz, 1.2 Hz), 7.20-7.24(m, 1H), 7.22(s, 2H), 7.58(s, 1H), 7.62(s, 1H), 8.49(d, 1H, J=4.9 Hz), 8.57(d, 1H, J=5.2 Hz).  97

55% 1.60-1.73(m, 4H), 1.82-1.93(m, 2H), 1.98-2.07(m, 2H), 2.87-2.97 (m, 2H), 3.12-3.22(m, 1H), 3.54 (s, 2H), 3.85(s, 3H), 3.89(s, 3H), 3.90(s, 3H), 3.93(s, 6H), 3.94(s, 6H), 4.39(s, 2H), 6.75(s, 2H), 6.79(dd, 1H, J=7.4 Hz, 7.41 Hz), 6.86(d, 1H, J=7.8 Hz), 6.97-7.05 (m, 2H), 7.13(s, 2H), 7.20(d, 1H, # J=4.7 Hz), 7.61(s, 1H), 7.75(s, 1H), 8.46-8.50(m, 2H), 8.68(d, 1H, J=2.0 Hz).  98

29% 1.64-1.82(m, 2H), 1.84-1.97(m, 2H), 2.00-2.15(m, 2H), 2.84-3.01 (m, 2H), 3.13-3.27(m, 1H), 3.56 (s, 2H), 3.82(s, 3H), 3.88(s, 3H), 3.90(s, 3H), 3.91(s, 6H), 3.96(s, 6H), 4.40(s, 2H), 6.63(s, 2H), 6.75-6.88(m, 2H), 6.97-7.04(m, 2H), 7.19(d, 1H, J=4.3 Hz), 7.25 # (s, 2H), 7.58-7.73(m, 2H), 8.50 (d, 1H, J=1.6 Hz), 8.56(d, 1H, J=2.2 Hz, 8.58 d, 1H, J=4.9 Hz).  99

30% 1.62-1.75(m, 2H), 1.83-1.94(m, 2H), 1.95-2.11(m, 2H), 2.84-3.01 (m, 2H), 3.12-3.23(m, 1H), 3.55 (s, 2H), 3.82(s, 3H), 3.88(s, 3H), 3.90(s, 3H), 3.90(s, 6H), 3.93(s, 6H), 4.39(s, 2H), 6.63(s, 2H), 6.70-6.86(m, 4H), 6.94-7.06(m, 2H), 7.68(s, 1H), 7.76(s, 1H), # 8.47(d, 1H, J=1.7 Hz), 8.49(d, 1H, J=1.7 Hz), 8.55(d, 1H, J=2.2 Hz), 8.69(s, 1H). 100

67% 1.64-1.79(m, 2H), 1.85-1.93(m, 2H), 1.99-2.09(m, 2H), 2.86-2.95 (m, 2H), 3.16-3.26(m, 1H), 3.52 (s, 2H), 3.84(s, 3H), 3.88(s, 3H), 3.90(s, 6H), 3.96(s, 6H), 4.40(s, 2H), 6.67(s, 2H), 6.78(dd, 1H, J=7.4 Hz, 7.4 Hz), 6.85(d, 1H, J=8.2 Hz), 6.97(dd, 1H, J=7.8 Hz, # 7.8 Hz), 7.02(dd, 1H, J=7.8, 1.6 Hz), 7.17-7.33(m, 6H), 7.44(s, 1H), 7.59(s, 1H), 8.57(d, 1H, J=5.1 Hz). 101

55% 1.62-1.77(m, 2H), 1.82-1.94(m, 2H), 1.98-2.08(m, 2H), 2.86-2.96 (m, 2H), 3.16-3.26(m, 1H), 3.54 (s, 2H), 3.83(s, 3H), 3.87(s, 3H), 3.90(s, 9H), 3.93(s, 6H), 4.39(s, 2H), 6.66(s, 2H), 6.73-6.80(m, 3H), 6.84(d, 1H, J=7.8 Hz), 6.97 (dd, 1H, J=7.8 Hz, 7.8 Hz), 7.01 # (d, 1H, J=7.8 Hz), 7.23-7.32(m, 3H), 7.43(s, 1H), 7.77(s, 1H), 8.47(d, 1H, J=1.4 Hz), 8.68(d, 1H, J=1.8 Hz).

The chemical names of the compounds of Examples 96 to 101 are:

EXAMPLE 96

 

4-[N-(2-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 97

 

4-[N-(2-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 98

 

4-[N-(2-Methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 99

 

4-[N-(2-Methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 100

 

4-[N-(2-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride EXAMPLE 101

 

4-[N-(2-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Dihydrochloride PREPARATION EXAMPLE 129 Synthesis of 1-(tert-Butoxycarbonyl)-4-[(2,3-dimethoxyphenyl)amino]piperidine

1-(tert-Butoxycarbonyl)-4-piperidone (4.78 g) and 2,3-dimethoxyaniline (3.68 g) were condensed in the same manner as described in Preparation Example 37 to give the title compound.

Yield: 3.18 g (39%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.29-1.42 (m, 2H), 1.45 (s, 9H), 1.97-2.03 (m, 2H), 2.92 (dt, 2H, J=13.5 Hz, 2.2 Hz), 3.38 (dt, 1H, J=13.8 Hz, 4.1 Hz), 3.77 (s, 3H), 3.82 (s, 3H), 3.99-4.03 (m, 2H), 4.17 (m, 1H), 6.27-6.32 (m, 2H), 6.88 (t, 1H, J=8.4 Hz).

PREPARATION EXAMPLE 130 Synthesis of 1-(tert-Butoxycarbonyl)-4-[(2,3-dimethoxyphenyl)amino]piperidine (673 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

1-(tert-Butoxycarbonyl)-4-(2,3-dimethoxyphenylamino)piperidine (673 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 613 mg (52%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.56-1.70 (m, 2H), 1.84-1.91 (m, 2H), 2.62-2.76 (m, 2H), 3.58 (tt, 1H, J=11.8 Hz, 3.6 Hz), 3.83 (s, 3H), 3.89 (s, 6H), 3.93 (s, 6H), 4.08-4.25 (m, 2H), 4.35 (s, 2H), 6.56-6.63 (m, 2H), 6.86 (t, 1H, J=8.3 Hz), 7.14 (s, 2H), 7.17 (dd, 1H, J=5.1 Hz, 1.2 Hz), 7.62 (s, 1H), 8.50 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 131 Synthesis of 4-[N-(2,3-Dimethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(2,3-dimethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (613 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 512 mg (88%).

EXAMPLE 102

 

Synthesis of 4-[N-(2,3-Dimethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride

4-[N-(2,3-Dimethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride (113 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (59 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as light yellow powder after converting a free base to a trihydrochloride.

Yield: 21 mg (12%). ¹H-NMR (400 MHz, measured as a free base, CDCl₃) δ: 1.76-1.96 (m, 4H), 2.00-2.13 (m, 2H), 2.86-3.00 (m, 2H), 3.42-3.60 (m, 1H), 3.54 (s, 2H), 3.82 (s, 3H), 3.88 (s, 3H), 3.90 (s, 3H), 3.97 (s, 6H), 4.41 (s, 2H), 6.57 (d, 1H, J=8.0 Hz), 6.62 (d, 1H, J=8.2 Hz), 6.85 (dd, 1H, J=8.4 Hz, 8.4 Hz), 7.11-7.29 (m, 6H), 7.59 (s, 1H), 7.63 (s, 1H), 8.50 (d, 1H, J=4.9 Hz), 8.59 (d, 1H, J=4.9 Hz).

PREPARATION EXAMPLE 132 Synthesis of 1-(tert-Butoxycarbonyl)-4-[4-[(trifluoromethoxy)phenyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-piperidone (5.00 g) and 4-(trifluoromethoxy)aniline (4.23 g) was treated in the same manner as described in Preparation Example 37 to give white powder of the title compound.

Yield: 5.22 g (60%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.25-1.40 (m, 2H), 1.47 (s, 9H), 1.98-2.08 (m, 2H), 2.83-2.98 (m, 2H), 3.34-3.43 (m, 1H), 3.97-4.12 (m, 2H), 6.58 (d, 2H, J=8.8 Hz), 7.03 (d, 2H, J=8.8 Hz).

PREPARATION EXAMPLE 133 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[4-(trifluoromethoxy)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[4-[(trifluoromethoxy)phenyl]amino]piperidine (721 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 543 mg (44%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.52-1.66 (m, 2H), 1.81-1.91 (m, 2H), 2.73-2.88 (m, 2H), 3.88-3.99 (m, 1H), 3.89 (s, 3H), 3.93 (s, 6H), 4.15-4.34 (m, 2H), 4.48 (s, 2H), 6.68 (d, 2H, J=9.2 Hz), 7.07 (d, 2H, J=8.6 Hz), 7.12 (dd, 1H, J=5.2 Hz, 1.3 Hz), 7.15 (s, 2H), 7.52 (s, 1H), 8.58 (d, 1H, J=5.2 Hz).

PREPARATION EXAMPLE 134 Synthesis of 4-[N-[4-(Trifluoromethoxy)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-[4-(trifluoromethoxy)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (543 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 481 mg (93%).

PREPARATION EXAMPLE 135 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[4-(trifluoromethoxy)phenyl]-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[4-[(trifluoromethoxy)phenyl]amino]piperidine (721 mg) and 5-chloromethyl-3-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 201 mg (16%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.54-1.67 (m, 2H), 1.82-1.90 (m, 2H), 2.74-2.86 (m, 2H), 3.84-3.91 (m, 1H), 3.88 (s, 3H), 3.89 (s, 6H), 4.16-4.30 (m, 2H), 4.52 (s, 2H), 6.67 (s, 2H), 6.72 (d, 2H, J=9.4 Hz), 7.06 (d, 2H, J=8.4 Hz), 7.64 (t, 1H, J=2.1 Hz), 8.49 (d, 1H, J=2.2 Hz), 8.68 (d, 1H, J=2.1 Hz).

PREPARATION EXAMPLE 136 Synthesis of 4-[N-[4-(Trifluoromethoxy)phenyl]-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl)methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-[4-(trifluoromethoxy)phenyl]-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine (201 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 185 mg (96%).

PREPARATION EXAMPLE 137 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[(4-trifluoromethoxy)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[4-[(trifluoromethoxy)phenyl]amino]piperidine (721 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (586 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 1.06 mg (86%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.56-1.68 (m, 2H), 1.83-1.90 (m, 2H), 2.71-2.86 (m, 2H), 3.87-3.90 (m, 1H), 3.88 (s, 3H), 3.89 (s, 6H), 4.16-4.29 (m, 2H), 4.51 (s, 2H), 6.70 (d, 2H, J=9.3 Hz), 6.70 (s, 2H), 7.04 (d, 2H, J=8.5 Hz), 7.22 (d, 1H, J=7.8 Hz), 7.34-7.44 (m, 3H).

PREPARATION EXAMPLE 138 Synthesis of 4-[N-[4-(Trifluoromethoxy)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperdine Hydrochloride

1-(tert-Butoxycarbonyl)-4-[N-[(4-trifluoromethoxy)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine (1.06 g) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 795 mg (84%).

EXAMPLES 103 TO 110

 

These compounds were obtained by the condensation of amines obtained in Preparation Examples 134, 136 and 138 with chloride derivatives obtained in Preparation Examples 3, 42 and 48. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Ex- am- NMR data (400 MHz, measured as ple Structure Yield free bases, CDCl₃) δ 103

70% 1.71-1.90(m, 4H), 2.15-2.23(m, 2H), 2.95-3.02(m, 2H), 3.58(s, 2H), 3.76-3.85(m, 1H), 3.89(s, 3H), 3.90(s, 3H), 3.92(s, 6H), 3.96(s, 6H), 4.54(s, 2H), 6.66(d, 2H, J=9.3 Hz), 7.05(d, 2H, J=8.5 Hz), 7.13(dd, 1H, J=5.1 Hz, 1.2 Hz), 7.14(s, 2H), 7.20(dd, 1H, # J=4.9 Hz, 1.2 Hz), 7.22(s, 2H), 7.53(s, 1H), 7.59(s, 1H), 8.57(d, 1H, J=4.9 Hz), 8.59(d, 1H, J=5.2 Hz). 104

48% 1.68-1.92(m, 4H), 2.13-2.25(m, 2H), 2.95-3.06(m, 2H), 3.60(s, 2H), 3.75-3.87(m, 1H), 3.89(s, 3H), 3.90(s, 3H), 3.91(s, 6H), 3.93(s, 6H), 4.52(s, 2H), 6.65(d, 2H, J=9.4 Hz), 6.75(s, 2H), 7.05 (d, 2H, J=9.2 Hz), 7.12(d, 1H, J=5.1 Hz), 7.14(s, 2H), 7.52(s, 1H), 7.76(s, 1H), 8.51(d, 1H, # J=1.8 Hz), 8.57(d, 1H, J=5.1 Hz), 8.70(d, 1H, J=2.1 Hz). 105

69% 1.70-1.89(m, 4H), 2.10-2.19(m, 2H), 2.98-3.08(m, 2H), 3.59(s, 2H), 3.72-3.84(m, 1H), 3.89(s, 6H), 3.92(s, 6H), 3.92(s, 6H), 4.52(s, 2H), 6.65(d, 2H, J=9.4 Hz), 6.76(s, 2H), 7.04(d, 2H, J=8.6 Hz), 7.11(d, 1H, J=5.1 Hz), 7.14(s, 2H), 7.25-7.33(m, 1H), 7.37(dd, 1H, J=7.4 Hz, 7.4 Hz), # 7.41-7.48(m, 2H), 7.51(s, 1H), 8.56(d, 1H, J=5.1 Hz). 106

41% 1.73-1.93(m, 4H), 2.12-2.26(m, 2H), 2.93-3.07(m, 2H), 3.53-3.65 (m, 2H), 3.74-3.84(m, 1H), 3.88 (s, 9H), 3.90(s, 3H), 3.96(s, 6H), 4.58(s, 2H), 6.66(s, 2H), 6.69(d, 2H, J=9.2 Hz), 7.05(d, 2H, J=8.8 Hz), 7.18-7.29(m, 3H), 7.59(br, 1H), 7.64(s, 1H), 8.49(s, 1H), # 8.60(d, 1H, J=5.3 Hz), 8.67(d, 1H, J=2.0 Hz). 107

28% 1.72-1.91(m, 4H), 2.12-2.28(m, 2H), 2.94-3.06(m, 2H), 3.60(s, 2H), 3.76-3.82(m, 1H), 3.88(s, 9H), 3.90(s, 3H), 3.93(s, 6H), 4.56(s, 2H), 6.65(s, 2H), 6.69(d, 2H, J=9.2 Hz), 6.75(s, 2H), 7.05 (d, 2H, J=8.8 Hz), 7.63(s, 1H), 7.76(s, 1H), 8.48(d, 1H, J=1.8 # Hz), 8.51(d, 1H, J=1.8 Hz), 8.66 (d, 1H, J=2.2 Hz), 8.70(d, 1H, J=2.2 Hz). 108

78% 1.76-1.91(m, 4H), 2.14-2.23(m, 2H), 2.94-3.03(m, 2H), 3.57(s, 2H), 3.75-3.84(m, 1H), 3.87(s, 9H), 3.90(s, 3H), 3.96(s, 6H), 4.56(s, 2H), 6.65-6.72(m, 4H), 7.03(d, 2H, J=8.8 Hz), 7.18-7.24 (m, 4H), 7.33-7.43(m, 3H), 7.59 (s, 1H), 8.59(d, 1H, J=4.9 Hz). 109

 5% 1.72-1.90(m, 4H), 2.12-2.21(m, 2H), 2.94-3.03(m, 2H), 3.59(s, 2H), 3.73-3.86(m, 1H), 3.87(s, 9H), 3.90(s, 3H), 3.93(s, 6H), 4.54(s, 2H), 6.66-6.70(m, 4H), 6.75(s, 2H), 7.03(d, 2H, J=9.0 Hz), 7.21(d, 1H, J=7.2 Hz), 7.32-7.41(m, 3H), 7.76(s, 1H), # 8.50(d, 1H, J=1.6 Hz), 8.69(d, 1H, J=1.6 Hz). 110

62% 1.72-1.89(m, 4H), 2.08-2.20(m, 2H), 2.97-3.07(m, 2H), 3.59(s, 2H), 3.73-3.83(m, 1H), 3.87(s, 9H), 3.89(s, 3H), 3.92(s, 6H), 4.55(s, 2H), 6.67(d, 2H, J=9.3 Hz), 6.69(s, 2H), 6.76(s, 2H), 7.02(d, 2H, J=8.6 Hz), 7.20(d, 1H, J=7.6 Hz), 7.25-7.47(m, 7H).

The chemical names of the compounds of Examples 103 to 110 are:

EXAMPLE 103

 

4-[N-[4-(Trifluoromethoxy)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 104

 

4-[N-[4-(Trifluoromethoxy)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 105

 

4-[N-[4-(Trifluoromethoxy)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Dihydrochloride EXAMPLE 106

 

4-[N-[4-(Trifluoromethoxy)phenyl]-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 107

 

4-[N-[4-(Trifluoromethoxy)phenyl]-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 108

 

4-[N-[4-(Trifluoromethoxy)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride EXAMPLE 109

 

4-[N-[4-(Trifluoromethoxy)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Dihydrochloride EXAMPLE 110

 

4-[N-[4-(Trifluoromethoxy)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Hydrochloride PREPARATION EXAMPLE 139 Synthesis of 1-(tert-Butoxycarbonyl)-4-[[4-(methylthio)phenyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-piperidone (5.00 g) and 4-(methylthio)aniline (3.33 g) was treated in the same manner as described in Preparation Example 37 to give white powder of the title compound.

Yield: 3.80 g (49%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.26-1.38 (m, 2H), 1.46 (s, 9H), 1.98-2.06 (m, 2H), 2.41 (s, 3H), 2.88-2.97 (m, 2H), 3.36-3.45 (m, 2H), 3.48-3.56 (br, 1H), 3.96-4.12 (m, 2H), 6.55 (d, 2H, J=8.8 Hz), 7.21 (d, 2H, J=8.8 Hz).

PREPARATION EXAMPLE 140 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[4-(methylthio)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[[4-(methylthio)phenyl]amino]piperidine (644 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 671 mg (58%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.50-1.66 (m, 2H), 1.81-1.89 (m, 2H), 2.40 (s, 3H), 2.74-2.87 (m, 2H), 3.88-3.94 (m, 1H), 3.90 (s, 3H), 3.94 (s, 6H), 4.15-4.29 (m, 2H), 4.48 (s, 2H), 6.67 (d, 2H, J=9.0 Hz), 7.11-7.18 (m, 1H), 7.16 (s, 2H), 7.22 (d, 2H, J=6.6 Hz), 7.54 (s, 1H), 8.57 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 141 Synthesis of 4-[N-[4-(Methylthio)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-[4-(methylthio)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (671 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 602 mg (94%).

PREPARATION EXAMPLE 142 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[4-(methylthio)phenyl]-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[[4-(methylthio)phenyl]amino]piperidine (645 mg) and 5-chloromethyl-3-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 312 mg (27%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.53-1.63 (m, 2H), 1.83-1.89 (m, 2H), 2.40 (s, 3H), 2.73-2.85 (m, 2H), 3.87-3.91 (m, 1H), 3.88 (s, 3H), 3.90 (s, 6H), 4.16-4.30 (m, 2H), 4.50 (s, 2H), 6.67 (s, 2H), 6.71 (d, 2H, J=9.0 Hz), 7.21 (d, 2H, J=9.0 Hz), 7.64 (s, 1H), 8.48 (d, 1H, J=2.2 Hz), 8.66 (d, 1H, J=2.1 Hz).

PREPARATION EXAMPLE 143 Synthesis of 4-[N-[4-(Methylthio)phenyl]-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-[4-(methylthio)phenyl]-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine (312 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 251 mg (84%).

PREPARATION EXAMPLE 144 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[(4-methylthio)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[[4-(methylthio)phenyl]amino]piperidine (645 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (586 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 1.10 g (95%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.55-1.68 (m, 2H), 1.81-1.90 (m, 2H), 2.39 (s, 3H), 2.73-2.86 (m, 2H), 3.87-3.91 (m, 1H), 3.88 (s, 3H), 3.89 (s, 6H), 4.15-4.29 (m, 2H), 4.50 (s, 2H), 6.68-6.73 (m, 4H), 7.19-7.24 (m, 3H), 7.33-7.43 (m, 3H).

PREPARATION EXAMPLE 145 Synthesis of 4-[N-[4-(Methylthio)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine Hydrochloride

1-(tert-Butoxycarbonyl)-4-[N-[4-(methylthio)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine (1.10 g) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 866 mg (89%).

EXAMPLES 111 TO 118

 

These compounds were obtained by the condensation of amines obtained in Preparation Examples 141, 143 and 145 with chloride derivatives obtained in Preparation Examples 3, 42 and 48. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Ex- am- NMR data (400 MHz, measured as ple Structure Yield free bases, CDCl₃) δ 111

40% 1.70-1.90(m, 4H), 2.14-2.26(m, 2H), 2.40(s, 3H), 2.94-3.04(m, 2H), 3.58(s, 2H), 3.76-3.88(m, 1H), 3.89(s, 3H), 3.90(s, 3H), 3.93(s, 6H), 3.96(s, 6H), 453(s, 2H), 6.66(d, 2H, J=9.0 Hz), 7.11-7.24(m, 8H), 7.54(s, 1H), 7.59(s, 1H), 8.56(d, 1H, J=5.1 Hz), 8.59(d, 1H, J=5.1 Hz). 112

53% 1.66-1.90(m, 4H), 2.12-2.24(m, 2H), 2.40(s, 3H), 2.94-3.05(m, 2H), 3.59(s, 2H), 3.73-3.88(m, 1H), 3.89(s, 3H), 3.90(s, 3H), 3.92(s, 6H), 3.93(s, 6H), 4.51(s, 2H), 6.65(d, 2H, J=8.8 Hz), 6.75 (s, 2H), 7.12(d, 1H, J=4.9 Hz), 7.14(s, 2H), 7.21(d, 2H, J=8.8 Hz), 7.53(s, 1H), 7.76(s, 1H), # 8.50(d, 1H, J=1.9 Hz), 6.55(d, 1H, J=4.9 Hz), 8.69(d, 1H, J=1.4 Hz). 113

53% 1.68-1.89(m, 4H), 2.10-2.20(m, 2H), 2.39(s, 3H), 2.98-3.07(m, 2H), 3.58(s, 2H), 3.75-3.87(m, 1H), 3.89(s, 6H), 3.92(s, 6H), 3.92(s, 6H), 4.51(s, 2H), 6.65(d, 2H, J=9.0 Hz), 6.76(s, 2H), 7.11 (d, 1H, J=5.1 Hz), 7.14(s, 2H), # 7.21(d, 2H, J=8.8 Hz), 7.29(d, 1H, J=7.4 Hz), 7.37(dd, 1H, J=7.6 Hz, 7.6 Hz), 7.42-7.49(m, 2H), 7.52(s, 1H), 8.54(d, 1H, J=4.9 Hz). 114

50% 1.57-2.00(m, 4H), 2.12-2.30(m, 2H), 2.39(s, 3H), 2.90-3.13(m, 2H), 3.50-3.74(m, 2H), 3.75-3.86 (m, 1H), 3.88(s, 3H), 3.89(s, 3H), 3.90(s, 6H), 3.97(s, 6H), 4.57(s, 2H), 6.66(s, 2H), 6.70(d, 2H, J=9.0 Hz), 7.17-7.30(m, 5H), 7.66(br, 2H), 8.48(s, 1H), 8.58-8.70(m, 2H). 115

59% 1.68-1.92(m, 4H), 2.12-2.27(m, 2H), 2.39(s, 3H), 2.94-3.08(m, 2H), 3.60(s, 2H), 3.74-3.83(m, 1H), 3.88(s, 3H), 3.89(s, 6H), 3.90(s, 3H), 3.93(s, 6H), 4.55(s, 2H), 6.66(s, 2H), 6.69(d, 2H, J=8.8 Hz), 6.73-6.80(m, 2H), 7.20 (d, 2H, J=8.8 Hz), 7.64(s, 1H), 7.77(br, 1H), 8.48(s, 1H), 8.50(s, # 1H), 8.65(s, 1H), 8.71(s, 1H). 116

85% 1.76-1.93(m, 4H), 2.14-2.24(m, 2H), 2.39(s, 3H), 2.94-3.03(m, 2H), 3.57(s, 2H), 3.76-3.86(m, 1H), 3.88(s, 6H), 3.90(s, 3H), 3.96(s, 6H), 4.55(s, 2H), 6.67-6.73(m, 4H), 7.18-7.29(m, 6H), 7.34(dd, 1H, J-7.6 Hz, 7.6 Hz), 7.37-7.44(m, 2H), 7.59(s, 1H), 8.59(d, 1H, J=4.9 Hz). 117

53% 1.72-1.90(m, 4H), 2.12-2.22(m, 2H), 2.39(s, 3H), 2.95-3.05(m, 2H), 3.59(s, 2H), 3.74-3.85(m, 1H), 3.87(s, 3H), 3.88(s, 6H), 3.89(s, 3H), 3.93(s, 6H), 4.54(s, 2H), 6.67-6.70(m, 4H), 6.75(s, 2H), 7.19-7.23(m, 3H), 7.33(dd, 1H, J=7.4 Hz, 7.4 Hz), 7.36-7.40 (m, 2H), 7.76(s, 1H), 8.50(d, 1H, # J=1.8 Hz), 8.69(s, 1H). 118

83% 1.72-1.90(m, 4H), 2.09-2.20(m, 2H), 2.38(s, 3H), 2.97-3.06(m, 2H), 3.58(s, 2H), 3.73-3.84(m, 1H), 3.87(s, 3H), 3.88(s, 3H), 3.89(s, 6H), 3.92(s, 6H), 4.54(s, 2H), 6.66-6.71(m, 4H), 6.76(s, 2H), 7.18-7.24(m, 3H), 7.26-7.48 (m, 7H).

The chemical names of the compounds of Examples 111 to 118 are:

EXAMPLE 111

 

1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methylthiophenyl)amino]piperidine Trihydrochloride EXAMPLE 112

 

1-[[3-(3,4,5-Trimethoxyphenyl)pyridin-5-yl]methyl]-4-[N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methylthiophenyl)amino]piperidine Trihydrochloride EXAMPLE 113

 

1-[3-(3,4,5-Trimethoxyphenyl)benzyl]-4-[N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methylthiophenyl)amino]piperidine Dihydrochloride EXAMPLE 114

 

1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]-N-(4-methylthiophenyl)amino]piperidine Trihydrochloride EXAMPLE 115

 

1-[[3-(3,4,5-Trimethoxyphenyl)pyridin-5-yl]methyl]-4-[N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]-N-(4-methylthiophenyl)amino]piperidine Trihydrochloride EXAMPLE 116

 

1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[3-(3,4,5-trimethoxyphenyl)benzyl]-N-(4-methylthiophenyl)amino]piperidine Dihydrochloride EXAMPLE 117

 

1-[[3-(3,4,5-Trimethoxyphenyl)pyridin-5-yl]methyl]-4-[N-[3-(3,4,5-trimethoxyphenyl)benzyl]-N-(4-methylthiophenyl)amino]piperidine Dihydrochloride EXAMPLE 118

 

1-[3-(3,4,5-Trimethoxyphenyl)benzyl]-4-[N-[3-(3,4,5-trimethoxyphenyl)benzyl]-N-(4-methylthiophenyl)amino]piperidine Hydrochloride PREPARATION EXAMPLE 146 Synthesis of 1-(tert-Butoxycarbonyl)-4-[(4-methylphenyl)amino]piperidine

1-(tert-Butoxycarbonyl)-4-piperidone (5.00 g) and p-toluidine (2.56 g) was treated in the same manner as described in Preparation Example 37 to give white powder of the title compound.

Yield: 5.79 g (83%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.25-1.36 (m, 2H), 1.46 (s, 9H), 1.99-2.06 (m, 2H), 2.23 (s, 3H), 2.86-2.96 (m, 2H), 3.30-3.43 (m, 2H), 3.96-4.10 (m, 2H), 6.53 (d, 2H, J=8.4 Hz), 6.98 (d, 2H, J=8.0 Hz).

PREPARATION EXAMPLE 147 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-methylphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(4-methylphenyl)amino]piperidine (581 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 1.00 g (91%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.55-1.59 (m, 2H), 1.81-1.90 (m, 2H), 2.23 (s, 3H), 2.72-2.86 (m, 2H), 3.81-3.94 (m, 1H), 3.89 (s, 3H), 3.93 (s, 6H), 4.14-4.30 (m, 2H), 4.45 (s, 2H), 6.66 (d, 2H, J=8.6 Hz), 7.02 (d, 2H, J=8.2 Hz), 7.13-7.16 (m, 3H), 7.55 (s, 1H), 8.55 (d, 1H, J=8.1 Hz).

PREPARATION EXAMPLE 148 Synthesis of 4-[N-(4-Methylphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-methylphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (1.00 g) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 924 mg (97%).

PREPARATION EXAMPLE 149 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-methylphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(4-methylphenyl)amino]piperidine (581 mg) and 5-chloromethyl-3-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 426 mg (39%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.52-1.70 (m, 2H), 1.82-1.90 (m, 2H), 2.23 (s, 3H), 2.72-2.86 (m, 2H), 3.77-3.86 (m, 1H), 3.88 (s, 3H), 3.90 (s, 6H), 4.10-4.28 (m, 2H), 4.47 (s, 2H), 6.67 (s, 2H), 6.70 (d, 2H, J=8.6 Hz), 7.01 (d, 2H, J=8.2 Hz), 7.67 (dd, 1H, J=2.1 Hz, 2.1 Hz), 8.50 (d, 1H, J=2.0 Hz), 8.64 (d, 1H, J=2.2 Hz).

PREPARATION EXAMPLE 150 Synthesis of 4-[N-(4-Methylphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-methylphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine (426 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 400 mg (99%).

PREPARATION EXAMPLE 151 Synthesis of 1-(tert-Butoxycarbonyl)4-[N-(4-methylphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(4-methylphenyl)amino]piperidine (581 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (586 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 1.03 g (94%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.44 (s, 9H), 1.50-1.66 (m, 2H), 1.83-1.90 (m, 2H), 2.23 (s, 3H), 2.72-2.85 (m, 2H), 3.82-3.92 (m, 1H), 3.88 (s, 3H), 3.89 (s, 6H), 4.11-4.30 (m, 2H), 4.47 (s, 2H), 6.68 (d, 2H, J=8.6 Hz), 6.71 (s, 2H), 7.00 (d, 2H, J=8.8 Hz), 7.23-7.27 (m, 1H), 7.32-7.44 (m, 3H).

PREPARATION EXAMPLE 152 Synthesis of 4-[N-(4-Methylphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine Hydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-methylphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine (1.03 g) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 882 mg (97%).

EXAMPLES 119 TO 126

 

These compounds were obtained by the condensation of amines obtained in Preparation Examples148, 150 and 152 with chloride derivatives obtained in Preparation Examples 3, 42 and 48. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Ex- am- NMR data (400 MHz, measured as ple Structure Yield free bases, CDCl₃) δ 119

66% 1.70-1.82(m, 2H), 1.83-1.91(m, 2H), 2.13-2.25(m, 2H), 2.23(s, 3H), 2.96-3.02(m, 2H), 3.57(s, 2H), 3.73-3.83(m, 1H), 3.89(s, 3H), 3.90(s, 3H), 3.93(s, 6H), 3.96(s, 6H), 4.50(s, 2H), 6.64 (d, 2H, J=8.8 Hz), 7.01(d, 2H, # j=8.5 Hz), 7.13-7.17(m, 3H), 7.20(d, 1H, J=4.9 Hz), 7.22(s, 2H), 7.56(s, 1H), 7.59(s, 1H), 8.54(d, 1H, J=5.1 Hz), 8.59(d, 1H, J=4.9 Hz). 120

41% 1.60-1.91(m, 4H), 2.12-2.24(m, 2H), 2.23(s, 3H), 2.95-3.05(m, 2H), 3.59(s, 2H), 3.73-3.83(m, 1H), 3.89(s, 3H), 3.89(s, 3H), 3.92(s, 6H), 3.93(s, 6H), 4.49 (s, 2H), 6.63(d, 2H, J=8.6 Hz), 6.75(s, 2H), 7.00(d, 2H, J=8.6 Hz), 7.13-7.16(m, 3H), 7.55(s, 1H), 7.76(s, 1H), 8.50(d, 1H, # J=1.8 Hz), 8.53(d, 1H, J=5.1 Hz), 8.70(s, 1H). 121

69% 1.67-1.80(m, 2H), 1.81 -1.89(m, 2H), 2.09-2.20(m, 2H), 2.22(s, 3H), 2.98-3.06(m, 2H), 3.58(s, 2H), 3.72-3.81(m, 1H), 3.88(s, 3H), 3.89(s, 3H), 3.92(s, 6H), 3.92(s, 6H), 4.49(s, 2H), 6.63 (d, 2H, J=8.4 Hz), 6.76(s, 2H), 7.00(d, 2H, J=8.6 Hz), 7.12-7.15(m, 3H), 7.26-7.32(m, # 1H), 7.37(dd, 1H, J=7.6 Hz, 7.6 Hz), 7.41-7.48(m, 2H), 7.55(s, 1H, 8.53(d, 1H, J=5.0 Hz. 122

47% 1.55-2.00(m, 4H), 2.12-2.31(m, 2H), 2.22(s, 3H), 2.93-3.10(m, 2H), 3.60(br, 2H), 3.69-3.80(m, 1H), 3.88(s, 3H), 3.89(s, 6H), 3.90(s, 3H), 3.96(s, 6H), 4.53(s, 2H), 6.66(s, 2H), 6.69(d, 2H, J=8.6 Hz), 7.00(d, 2H, J=8.6 Hz), 7.19-7.27(m, 4H), 7.68(s, 1H), 8.50(s, 1H), 8.60 # (d, 1H, J=4.9 Hz), 8.64(d, 1H, J=2.2 Hz). 123

34% 1.67-1.98(m, 4H), 2.10-2.38(m, 2H), 2.22(s, 3H), 2.85-3.10(m, 2H), 3.53-3.67(s, 2H), 3.67-3.79 (m, 1H), 3.88(s, 3H), 3.89(s, 6H), 3.90(s, 3H), 3.93(s, 6H), 4.51(s, 2H), 6.66(s, 2H), 6.68 (d, 2H, J=8.8 Hz), 6.76(s, 2H), 7.00(d, 2H, J=8.2 Hz), 7.67(s, 1H), 7.77(br, 1H), 8.47-8.53(m, # 2H), 8.63(d, 1H, J=2.0 Hz), 8.70 s, 1H). 124

91% 1.73-1.92(m, 4H), 2.12-2.26(m, 2H), 2.21(s, 3H), 2.92-3.02(m, 2H), 3.57(s, 2H), 3.72-3.82(m, 1H), 3.87(s, 3H), 3.88(s, 6H), 3.90(s, 3H), 3.95(s, 6H), 4.53 (s, 2H), 6.67(d, 2H, J=7.8 Hz), 6.70(s, 2H), 6.99(d, 2H, J=8.0 Hz), 7.18-7.25(m, 4H), 7.33 (dd, 1H, J=7.4 Hz, 7.4 Hz), 7.38 # (d, 1H, J=7.2 Hz), 7.42(s, 1H), 7.59(s, 1H), 8.58(d, 1H, J=4.7 Hz). 125

74% 1.70-1.92(m, 4H), 2.10-2.28(m, 2H), 2.21(s, 3H), 2.92-3.06(m, 2H), 3.58(s, 2H), 3.72-3.82(m, 1H), 3.87(s, 3H), 3.88(s, 6H), 3.89(s, 3H), 3.93(s, 6H), 4.51 (s, 2H), 6.66(d, 2H, J=8.6 Hz), 6.70(s, 2H), 6.75(s, 2H), 7.23 (d, 1H, J=7.0 Hz), 7.32(dd, 1H, J=7.6 Hz, 7.6 Hz), 7.37(d, 1H, # J=7.8 Hz), 7.41(s, 1H), 7.77(s, 1H), 8.49(s, 1H), 8.69(s, 1H). 126

84% 1.71-1.88(m, 4H), 2.08-2.18(m, 2H), 2.21(s, 3H), 2.96-3.04(m, 2H), 3.58(s, 2H), 3.71-3.83(m, 1H), 3.87(s, 3H), 3.88(s, 6H), 3.89(s, 3H), 3.92(s, 6H), 4.52 (s, 2H), 6.66(d, 2H, J=8.6 Hz), 6.70(s, 2H), 6.76(s, 2H), 6.98 (d, 2H, J=8.3 Hz), 7.22-7.47(m, 8H).

The chemical names of the compounds of Examples 119 to 126 are:

EXAMPLE 119

 

1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methylphenyl)amino]piperidine Trihydrochloride EXAMPLE 120

 

1-[[3-(3,4,5-Trimethoxyphenyl)pyridin-5-yl]methyl]-4-[N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methylphenyl)amino]piperidine Trihydrochloride EXAMPLE 121

 

1-[3-(3,4,5-trimethoxyphenyl)benzyl]-4-[N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methylphenyl)amino]piperidine Dihydrochloride EXAMPLE 122

 

1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]-N-(4-methylphenyl)amino]piperidine Trihydrochloride EXAMPLE 123

 

1-[[3-(3,4,5-Trimethoxyphenyl)pyridin-5-yl]methyl]-4-[N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]-N-(4-methylphenyl)amino]piperidine Trihydrochloride EXAMPLE 124

 

1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[3-(3,4,5-trimethoxyphenyl)benzyl]-N-(4-methylphenyl)amino]piperidine Dihydrochloride EXAMPLE 125

 

1-[[3-(3,4,5-Trimethoxyphenyl)pyridin-5-yl]methyl]-4-[N-[3-(3,4,5-trimethoxyphenyl)benzyl]-N-(4-methylphenyl)amino]piperidine Dihydrochloride EXAMPLE 126

 

1-[3-(3,4,5-Trimethoxyphenyl)benzyl]-4-[N-[3-(3,4,5-trimethoxyphenyl)benzyl]-N-(4-methylphenyl)amino]piperidine Hydrochloride PREPARATION EXAMPLE 153 Synthesis of 1-(tert-Butoxycarbonyl)-4-[[4-(trifluoromethyl)phenyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-piperidone (5.00 g) and 4-(trifluoromethyl)aniline (3.85 g) was treated in the same manner as described in Preparation Example 37 to give white powder of the title compound.

Yield: 3.30 g (40%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.30-1.41 (m, 2H), 1.47 (s, 9H), 2.00-2.07 (m, 2H), 2.88-2.99 (m, 2H), 3.32-3.52 (m, 1H), 3.83-3.89 (m, 1H), 4.00-4.14 (m, 2H), 6.59 (d, 2H, J=8.4 Hz), 7.39 (d, 2H, J=8.4 Hz).

PREPARATION EXAMPLE 154 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[4-(trifluoromethyl)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[[4-(trifluoromethyl)phenyl]amino]piperidine (688 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 412 mg (34%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.54-1.68 (m, 2H), 1.81-1.90 (m, 2H), 2.77-2.90 (m, 2H), 3.89 (s, 3H), 3.92 (s, 6H), 3.98-4.07 (m, 1H), 4.18-4.33 (m, 2H), 4.55 (s, 2H), 6.73 (d, 2H, J=8.8 Hz), 7.09 (d, 1H, J=3.7 Hz), 7.13 (s, 2H), 7.44 (d, 2H, J=8.8 Hz), 7.49 (s, 1H), 8.58 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 155 Synthesis of 4-[N-[4-(Trifluoromethyl)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-[4-(trifluoromethyl)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (412 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 359 mg (91%).

PREPARATION EXAMPLE 156 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[(4-trifluoromethyl)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[[4-(trifluoromethyl)phenyl]amino]piperidine (689 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (586 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 522 mg (44%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.58-1.70 (m, 2H), 1.83-1.90 (m, 2H), 2.76-2.87 (m, 2H), 3.87 (s, 6H), 3.88 (s, 3H), 3.96-4.06 (m, 1H), 4.15-4.30 (m, 2H), 4.58 (s, 2H), 6.68 (s, 2H), 6.76 (d, 2H, J=8.8 Hz), 7.19 (s, 1H, J=7.4 Hz), 7.33-7.44 (m, 5H).

PREPARATION EXAMPLE 157 Synthesis of 4-[N-[4-(Trifluoromethyl)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine Hydrochloride

1-(tert-Butoxycarbonyl)-4-[N-[4-(trifluoromethyl)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine (522 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 460 mg (99%).

EXAMPLES 127 TO 132

 

These compounds were obtained by the condensation of amines obtained in Preparation Examples 155 and 157 with chloride derivatives obtained in Preparation Examples 3, 42 and 48. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Ex- am- NMR data (400 MHz, measured as ple Structure Yield free bases, CDCl₃) δ 127

72% 1.74-1.92(m, 4H), 2.17-2.26(m, 2H), 2.96-3.04(m, 2H), 3.59(s, 2H), 3.89(s, 3H), 3.90(s, 3H), 3.91(s, 6H), 3.96(s, 6H), 4.60(s, 2H), 6.72(d, 2H, J=8.8 Hz), 7.10 (d, 1H, J=4.9 Hz), 7.13(s, 2H), 7.20(d, 1H, J=5.1 Hz), 7.43(d, 2H, J=8.8 Hz), 7.50(s, 1H), 7.59 # (s, 1H), 8.56(d, 1H, J=4.9 Hz), 8.58(d, 1H, J=5.1 Hz). 128

51% 1.70-1.90(m, 4H), 2.14-2.28(m, 2H), 2.96-3.08(m, 2H), 3.61(s, 2H), 3.87-3.96(m, 1H), 3.89(s, 3H), 3.90(s, 3H), 3.91(s, 6H), 3.93(s, 6H), 4.59(s, 2H), 6.71(d, 2H, J=8.8 Hz), 6.75(s, 2H), 7.07-7.15(m, 3H), 7.43(d, 2H, J=8.8 Hz), 7.49(s, 1H), 7.76(s, 1H), 8.51(d, 1H, J=1.8 Hz), 8.57 # (d, 1H, J=5.1 Hz), 8.70(s, 1H). 129

59% 1.72-1.88(m, 4H), 2.11-2.24(m, 2H), 2.98-3.10(m, 2H), 3.59(s, 2H), 3.87-3.95(m, 1H), 3.88(s, 3H), 3.89(s, 3H), 3.90(s, 6H), 3.92(s, 6H), 4.59(s, 2H), 6.71(d, 2H, J=9.0 Hz), 6.76(s, 2H), 7.08 (d, 1H, J=5.1 Hz), 7.12(s, 2H), 7.29(d, 1H, J=7.4 Hz), 7.37(dd, # 1H, J=7.6 Hz, 7.6 Hz), 7.40-7.52 (m, 5H), 8.56(d, 1H, J=5.1 Hz). 130

81% 1.78-1.94(m, 4H), 2.15-2.27(m, 2H), 2.94-3.08(m, 2H), 3.58(s, 2H), 3.86(s, 6H), 3.87(s, 3H), 3.90(s, 3H), 3.96(s, 6H), 4.63(s, 2H), 6.67(s, 2H), 6.74(d, 2H, J=8.8 Hz), 7.17-7.24(m, 4H), 7.34-7.45(m, 5H), 7.59(s, 1H), 8.59(d, 1H, J=5.1 Hz. 131

54% 1.75-1.90(m, 4H), 2.14-2.24(m, 2H), 2.95-3.04(m, 2H), 3.60(s, 2H), 3.84-3.88(m, 1H), 3.86(m, 1H), 3.87(s, 3H), 3.90(s, 3H), 3.93(s, 6H), 4.61(s, 2H), 6.67(s, 2H), 6.72-6.77(m, 4H), 7.18(d, 1H, J=7.4 Hz), 7.33-7.43(m, 5H), 7.76(s, 1H), 8.50(d, 1H, J=1.9 Hz), 8.69(d, 1H, J=1.9 Hz). 132

67% 1.76-1.88(m, 4H), 2.11-2.19(m, 2H), 2.98-3.06(m, 2H), 3.59(s, 2H), 3.86(s, 6H), 3.87(s, 3H), 3.89(s, 3H), 3.92(s, 6H), 4.61(s, 2H), 6.67(s, 2H), 6.73(d, 2H, J=8.8 Hz), 6.76(s, 2H), 7.18(d, 1H, J=7.3 Hz), 7.29(d, 1H, J=7.6 Hz), 7.32-7.47 m, 8H).

The chemical names of the compounds of Examples 127 to 132 are:

EXAMPLE 127

 

4-[N-[4-(Trifluoromethyl)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 128

 

4-[N-[4-(Trifluoromethyl)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 129

 

4-[N-[4-(Trifluoromethyl)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Dihydrochloride EXAMPLE 130

 

4-[N-[4-(Trifluoromethyl)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride EXAMPLE 131

 

4-[N-[4-(Trifluoromethyl)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Dihydrochloride EXAMPLE 132

 

4-[N-[4-(Trifluoromethyl)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Hydrochloride PREPARATION EXAMPLE 158 Synthesis of 4-(4-Bromophenyl)amino-1-(tert-butoxycarbonyl)piperidine

1-(tert-Butoxycarbonyl)-4-piperidone (5.00 g) and 4-bromoaniline (4.11 g) was treated in the same manner as described in Example 37 to give white crystalline powder of the title compound.

Yield: 3.09 g (36%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.25-1.37 (m, 2H), 1.46 (s, 9H), 1.97-2.05 (m, 2H), 2.86-2.96 (m, 2H), 3.33-3.42 (m, 2H), 3.47-3.57 (m, 1H), 3.96-4.12 (m, 2H), 6.47 (d, 2H, J=8.8 Hz), 7.24 (d, 2H, J=9.0 Hz).

PREPARATION EXAMPLE 159 Synthesis of 4-[N-(4-Bromophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-(tert-butoxycarbonyl)piperidine

4-(4-Bromophenyl)amino-l-(tert-butoxycarbonyl)piperidine (711 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 607 mg (50%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.50-1.64 (m, 2H), 1.81-1.88 (m, 2H), 2.74-2.88 (m, 2H), 3.86-3.94 (m, 1H), 3.89 (s, 3H), 3.93 (s, 6H), 4.14-4.32 (m, 2H), 4.46 (s, 2H), 6.59 (d, 2H, J=9.1 Hz), 7.10 (d, 1H, J=5.2 Hz), 7.14 (s, 2H), 7.28 (d, 2H, J=9.1 Hz), 7.50 (s, 1H), 8.57 (d, 1H, J=5.0 Hz).

PREPARATION EXAMPLE 160 Synthesis of 4-[N-(4-Bromophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

4-[N-(4-Bromophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-(tert-butoxycarbonyl)piperidine (607 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 541 mg (93%).

PREPARATION EXAMPLE 161 Synthesis of 4-[N-(4-Bromophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-(tert-butoxycarbonyl)piperidine

4-(4-Bromophenyl)amino-1-(tert-butoxycarbonyl)piperidine (711 mg) and 5-chloromethyl-3-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 347 mg (28%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.52-1.67 (m, 2H), 1.80-1.89 (m, 2H), 2.72-2.87 (m, 2H), 3.82-3.92 (m, 1H), 3.89 (s, 3H), 3.90 (s, 6H), 4.14-4.33 (m, 2H), 4.50 (s, 2H), 6.63 (d, 2H, J=9.2 Hz), 6.65 (s, 2H), 7.28 (d, 2H, J=9.4 Hz), 7.61 (s, 1H), 8.47 (d, 1H, J=2.0 Hz), 8.67 (d, 1H, J=2.2 Hz).

PREPARATION EXAMPLE 162 Synthesis of 4-[N-(4-Bromophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine Dihydrochloride

4-[N-(4-Bromophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-(tert-butoxycarbonyl)piperidine (347 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 302 mg (91%).

PREPARATION EXAMPLE 163 Synthesis of 4-[N-(4-Bromophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-(tert-butoxycarbonyl)piperidine

4-(4-Bromophenyl)amino-1-(tert-butoxycarbonyl)piperidine (711 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (586 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 1.14 g (93%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.52-1.67 (m, 2H), 1.80-1.89 (m, 2H), 2.72-2.86 (m, 2H), 3.84-3.91 (m, 1H), 3.88 (s, 3H), 3.89 (s, 6H), 4.11-4.32 (m, 2H), 4.49 (s, 2H), 6.62 (d, 2H, J=9.2 Hz), 6.69 (s, 2H), 7.19 (d, 1H, J=7.6 Hz), 7.25 (d, 2H, J=5.5 Hz), 7.32-7.42 (m, 3H).

PREPARATION EXAMPLE 164 Synthesis of 4-[N-(4-Bromophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine Hydrochloride

4-[N-(4-Bromophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-(tert-butoxycarbonyl)piperidine (1.14 g) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 973 mg (84%).

EXAMPLES 133 TO 140

 

These compounds were obtained by the condensation of amines obtained in Preparation Examples 160, 162 and 164 with chloride derivatives obtained in Preparation Examples 3, 42 and 48. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Ex- am- NMR data (400 MHz, measured as ple Structure Yield free bases, CDCl₃) δ 133

52% 1.70-1.90(m, 4H), 2.14-2.25(m, 2H), 2.94-3.04(m, 2H), 3.58(s, 2H), 3.73-3.84(m, 1H), 3.89(s, 3H), 3.90(s, 3H), 3.92(s, 6H), 3.96(s, 6H), 4.52(s, 2H), 6.57(d, 2H, J=8.8 Hz), 7.10(d, 1H, J=4.9 Hz), 7.14(s, 2H), 7.20(d, 1H, J=4.9 Hz), 7.22(s, 2H), 7.26(d, # 2H, J=8.5 Hz), 7.51(s, 1H), 7.59 (s, 1H), 8.56(d, 1H, J=4.9 Hz), 8.59(d, 1H, J=4.9 Hz). 134

56% 1.68-1.88(m, 4H), 2.12-2.24(m, 2H), 2.95-3.04(m, 2H), 3.59(s, 2H), 3.72-3.84(m, 1H), 3.89(s, 3H), 3.90(s, 3H), 3.92(s, 6H), 3.93(s, 6H), 4.50(s, 2H), 6.57(d, 2H, J=9.2 Hz), 6.74(s, 2H), 7.09 (d, 1H, J=3.9 Hz), 7.13(s, 2H), 7.26(d, 2H, J=8.8 Hz), 7.50(s, # 1H), 7.75(s, 1H), 8.50(d, 1H, J=2.0 Hz), 8.55(d, 1H, J=5.0 Hz), 8.69(d, 1H, J=2.0 Hz). 135

65% 1.70-1.86(m, 4H), 2.10-2.20(m, 2H), 2.97-3.08(m, 2H), 3.59(s, 2H), 3.72-3.82(m, 1H), 3.89(s, 6H), 3.92(s, 6H), 3.92(s, 6H), 4.50(s, 2H), 6.56(d, 2H, J=9.2 Hz), 6.76(s, 2H), 7.09(d, 1H, J=5.1 Hz), 7.13(s, 2H), 7.23-7.33 (m, 3H), 7.37(dd, 1H, J=7.4 Hz), 7.41-7.48(m, 2H), 7.49(s, 1H), # 8.54(d, 1H, J=5.1 Hz). 136

49% 1.77-1.93(m, 4H), 2.12-2.30(m, 2H), 2.94-3.10(m, 2H), 3.60(s, 2H), 3.73-3.83(m, 1H), 3.88(s, 3H), 3.89(s, 6H), 3.90(s, 3H), 3.96(s, 6H), 4.55(s, 2H), 6.61(d, 2H, J=9.2 Hz), 6.65(s, 2H), 7.19-7.29(m, 5H), 7.62(br, 2H), 8.47(d, 1H, J=1.6 Hz), 8.60(d, # 1H, J=4.9 Hz), 8.66(d, 1H, J=2.0 Hz). 137

50% 1.70-1.92(m, 4H), 2.12- 2.27(m, 2H), 2.93-3.07 (m, 2H), 3.60(s, 2H), 3.67-4.08(m, 1H), 3.88(s, 3H), 3.89(s, 6H), 3.90(s, 3H), 3.93(s, 6H), 4.54(s, 2H), 6.60(d, 2H, J=9.0 Hz), 6.64(s, 2H), 6.73- 6.80(m, 2H), 7.25(s, 2H), 7.61(s, 1H), 7.77(br, # 1H), 8.45(d, 1H, J=1.7 Hz), 8.50(d, 1H, J=1.7 Hz), 8.65(d, 1H, J=2.0 Hz). 138

81% 1.75-1.90(m, 4H), 2.17- 2.24(m, 2H), 2.94-3.02 (m, 2H), 3.57(s, 2H), 3.72-3.83(m, 1H), 3.88(s, 3H), 3.88(s, 6H), 3.90(s, 3H), 3.95(s, 6H), 4.54(s, 2H), 6.60(d, 2H, J=9.2 Hz), 6.69(s, 2H), 7.18- 7.27(m, 6H), 7.32-7.42 (m, 3H), 7.60(s, 1H), 8.58 # (d, 1H, J=4.9 Hz). 139

80% 1.72-1.90(m, 4H), 2.13- 2.21(m, 2H), 2.94-3.05 (m, 2H), 3.59(s, 2H), 3.72-3.82(m, 1H), 3.87(s, 3H), 3.88(s, 6H), 3.89(s, 3H), 3.93(s, 6H), 4.53(s, 2H), 6.60(d, 2H, J=9.0 Hz), 6.68(s, 2H), 6.75(s, 2H), 7.19(d, 1H, J=7.2 Hz), 7.24(d, 2H, J=9.0 # Hz), 7.31-7.41(m, 3H), 7.76(s, 1H), 8.50(d, 1H, J=1.8 Hz), 8.70(s, 1H). 140

78% 1.72-1.88(m, 4H), 2.08- 2.18(m, 2H), 2.97-3.06 (m, 2H), 3.58(s, 2H), 3.71-3.82(m, 1H), 3.87 (s, 3H), 3.88(s, 6H), 3.89 (s, 3H), 3.92(s, 6H), 4.53 (s, 2H), 6.59(d, 2H, J=9.3 Hz), 6.68(s, 2H), 6.76(s, 2H), 7.18(d, 1H, J=7.3 # Hz), 7.21-7.47(m, 9H)

The chemical names of the compounds of Examples 133 to 140 are:

EXAMPLE 133

 

4-[N-(4-Bromophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 134

 

4-[N-(4-Bromophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 135

 

4-[N-(4-Bromophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Dihydrochloride EXAMPLE 136

 

4-[-(4-Bromophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 137

 

4-[N-(4-Bromophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 138

 

4-[N-(4-Bromophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride EXAMPLE 139

 

4-[N-(4-Bromophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Dihydrochloride EXAMPLE 140

 

4-[N-(4-Bromophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Hydrochloride PREPARATION EXAMPLE 165 Synthesis of 1-(tert-Butoxycarbonyl)-4-[(4-chlorophenyl)amino]piperidine

1-(tert-Butoxycarbonyl)-4-piperidone (5.00 g) and 4-chloroaniline (3.05 g) was treated in the same manner as described in Preparation Example 37 to give white powder of the title compound.

Yield: 3.80 g (49%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.24-1.38 (m, 2H), 1.46 (s, 9H), 1.97-2.05 (m, 2H), 2.86-2.96 (m, 2H), 3.32-3.42 (m, 2H), 3.51 (br, 1H), 6.52 (d, 2H, J=9.0 Hz), 7.11 (d, 2H, J=9.0 Hz).

PREPARATION EXAMPLE 166 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-chlorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(4-chlorophenyl)amino]piperidine (621 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 789 mg (69%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.51-1.68 (m, 2H), 1.80-1.89 (m, 2H), 2.72-2.86 (m, 2H), 3.87-3.90 (m, 1H), 3.89 (s, 3H), 3.93 (s, 6H), 4.64 (s, 2H), 6.64 (d, 2H, J=9.0 Hz), 7.14 (d, 1H, J=5.3 Hz), 7.15 (d, 2H, J=9.0 Hz), 7.51 (s, 2H), 8.57 (d, 2H, J=5.1 Hz).

PREPARATION EXAMPLE 167 Synthesis of 4-[N-(4-Chlorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-chlorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (789 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 673 mg (90%).

PREPARATION EXAMPLE 168 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-chlorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(4-chlorophenyl)amino]piperidine (621 mg) and 5-chloromethyl-3-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 268 mg (24%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.56-1.76 (m, 2H), 1.80-1.90 (m, 2H), 2.76-2.83 (m, 2H), 3.86-3.90 (m, 1H), 3.89 (s, 3H), 3.90 (s, 6H), 4.15-4.30 (m, 2H), 4.50 (s, 2H), 6.66 (s, 2H), 6.68 (d, 2H, J=9.2 Hz), 7.15 (d, 2H, J=9.0 Hz), 7.63 (s, 1H), 8.47 (d, 1H, J=2.0 Hz), 8.66 (d, 1H, J=2.0 Hz).

PREPARATION EXAMPLE 169 Synthesis of 4-[N-(4-Chlorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-chlorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine (268 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 233 mg (91%).

PREPARATION EXAMPLE 170 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-chlorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[4-(chlorophenyl)amino]piperidine (622 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (586 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 1.04 g (92%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.58-1.67 (m, 2H), 1.82-1.91 (m, 2H), 2.74-2.86 (m, 2H), 3.85-3.92 (m, 1H), 3.88 (s, 3H), 3.89 (s, 6H), 4.35-4.31 (m, 2H), 4.49 (s, 2H), 6.66 (d, 2H, J=9.2 Hz), 6.70 (s, 2H), 7.12 (d, 2H, J=9.0 Hz), 7.20 (d, 2H, J=7.3 Hz), 7.33-7.43 (m, 3H).

PREPARATION EXAMPLE 171 Synthesis of 4-[N-(4-Chlorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine Hydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-chlorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine (1.04 g) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 899 mg (97%).

EXAMPLES 141 TO 148

 

These compounds were obtained by the condensation of amines obtained in Preparation Examples 167, 169 and 171 with chloride derivatives obtained in Preparation Examples 3, 42 and 48. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Ex- NMR data (400 MHz, mea- ample Structure Yield sured as free bases, CDCl₃) δ 141

66% 1.71-1.90(m, 4H), 2.15-2.24 (m, 2H), 2.95-3.05(m, 2H), 3.58(s, 2H), 3.73-3.84(m, 1H), 3.89(s, 3H), 3.90(s, 3H), 3.93(s, 6H), 3.96(s, 6H), 4.52(s, 2H), 6.62(d, 2H, J= 9.0Hz), 7.10-7.16(m, 5H), 7.19-7.24(m, 3H), 7.52(s, 1H), 7.59(s, 1H), 8.56(d, 1H, J=4.9Hz), 8.59(d, 1H, J= 4.9Hz). 142

67% 1.69-1.90(m, 1H), 2.12-2.25 (m, 2H), 2.93-3.06(m, 2H), 3.59(s, 2H), 3.72-3.83(m, 1H), 3.89(s, 3H), 3.90(s, 3H), 3.92(s, 6H), 3.93(s, 6H), 4.50(s, 2H), 6.62(d, 2H, J= 9.2Hz), 6.75(s, 2H), 7.10(d, 1H, J=5.3Hz), 7.13(s, 2H), 7.13(d, 2H, J=9.0Hz), 7.50(s, 1H), 7.76(s, 1H), 8.50(d, 1H, J=1.8Hz), 8.55(d, 1H, J= 5.1Hz), 8.70(d, 1H, J= 1.8Hz). 143

70% 1.65-1.88(m, 4H), 2.08-2.20 (m, 2H), 2.97-3.07(m, 2H), 3.59(s, 2H), 3.71-3.82(m, 1H), 3.88(s, 3H), 3.89(s, 3H), 3.90-3.93(m, 3H), 4.50(s, 2H), 6.61(d, 2H, J= 8.2Hz), 6.76(s, 2H), 7.07-7.14(m, 5H), 7.28(d, 1H, J=6.6Hz), 7.37(dd, 1H, J=7.4Hz), 7.40-7.47(m, 2H), 7.50(s, 1H), 8.54(d, 1H, J=5.1Hz). 144

57% 1.56-1.93(m, 4H), 2.12—2.30 (m, 2H), 2.92-3.10(m, 2H), 3.53-3.68(m, 2H),3.70- 3.82(m, 1H), 3.88(s, 3H), 3.89 (s, 6H), 3.90(s, 3H), 3.96(s, 6H), 4.56(s, 2H), 6.64-6.70 (m, 4H), 7.13(d, 2H), J= 9.0Hz), 7.20-7.30(m, 3H), 7.63(br, 2H), 8.48(s, 1H), 8.60(d, 1H, J=5.1Hz), 8.66(d, 1H, J=2.2Hz). 145

70% 1.71-1.92(m, 4H), 2.12—2.27 (m, 2H), 2.94-3.07(m, 2H), 3.59(s, 2H), 3.69-3.81(s, 1H), 3.88(s, 3H), 3.89(s, 6H), 3.90(s, 3H), 3.93(s, 6H), 4.54(s, 2H), 6.63-6.68(m, 4H), 6.75(s, 2H), 7.13(d, 2H, J=9.0Hz), 7.62(s, 1H), 7.76 (s, 1H), 8.47(d, 1H, J= 1.8Hz), 8.50(d, 1H, J= 1.8Hz), 8.65(d, 1H, J=2.0Hz), 8.70(s, 1H). 146

78% 1.75-1.91(m, 4H), 2.13-2.23 (m, 2H), 2.94-3.02(m, 2H), 3.57(s, 2H), 3.73-3.82(m, 1H), 3.88(s, 3H), 3.88(s, 6H), 3.90(s, 3H), 3.96(s, 6H), 4.55(s, 2H), 6.65(d, 2H, J= 9.0Hz), 6.68(s, 2H), 7.11(d, 2H, J=8.5Hz), 7.18-7.24 (m, 4H), 7.32-7.42(m, 3H), 7.59(s, 1H), 8.59(d, 1H, J= 4.9Hz). 147

63% 1.72-1.89(m, 4H), 2.12-2.21 (m, 2H), 2.94-3.03(m, 2H), 3.59(s, 2H), 3.72-3.82(m, 1H), 3.87(s, 3H), 3.88(s, 6H), 3.90(s, 3H), 3.93(s, 6H), 4.53(s, 2H), 6.64(d, 2H, J= 9.2Hz), 6.68(s, 2H), 6.75(s, 2H), 7.11(d, 2H), (d, 2H), 7.19(d, 1H, J= 7.6Hz), 7.32-7.40(m, 3H), 7.76(s, 1H), 8.50(d, 1H, J=1.8Hz), 8.69(d, 1H, J= 2.2Hz). 148

68% 1.72-1.87(m, 4H), 2.08-2.18 (m, 2H), 2.97-3.05(m, 2H), 3.58(s, 2H), 3.71-3.82(m, 1H), 3.87(s, 3H), 3.88(s, 6H), 3.89(s, 3H), 3.92(s, 6H), 4.53(s, 2H), 6.64(dt, 2H, J= 9.3Hz, 2.9Hz), 6.68(s, 2H), 6.76(s, 2H), 7.10(dt, 2H, J=9.0Hz, 2.8Hz), 7.19(d, 1H, J=7.6Hz), 7.24-7.47(m, 7H).

The chemical names of the compounds of Examples 141 to 148 are:

EXAMPLE 141

 

4-[N-(4-Chlorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 142

 

4-[N-(4-Chlorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 143

 

4-[N-(4-Chlorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Dihydrochloride EXAMPLE 144

 

4-[N-(4-Chlorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 145

 

4-[N-(4-Chlorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 146

 

4-[N-(4-Chlorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride EXAMPLE 147

 

4-[N-(4-Chlorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Dihydrochloride EXAMPLE 148

 

4-[N-(4-Chlorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Hydrochloride PREPARATION EXAMPLE 172 Synthesis of 1-(tert-Butoxycarbonyl)-4-[(3,4-difluorophenyl)amino]piperidine

1-(tert-Butoxycarbonyl)-4-piperidone (5.00 g) and 3,4-difluoroaniline (3.09 g) was treated in the same manner as described in Preparation Example 37 to give light brown prism crystal of the title compound.

Yield: 4.66 g (62%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.24-1.37 (m, 2H), 1.46 (s, 9H), 1.97-2.05 (m, 2H), 2.85-2.96 (m, 2H), 3.26-3.36 (m, 1H), 3.38-3.52 (m, 1H), 3.96-4.14 (m, 2H), 6.22-6.28 (m, 1H), 6.38 (ddd, 1H, J=12.7 Hz, 6.6 Hz, 2.9 Hz), 6.94 (dd, 1H, J=19.1 Hz, 9.0 Hz).

PREPARATION EXAMPLE 173 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(3,4-difluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(3,4-difluorophenyl)amino]piperidine (625 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 534 mg (47%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.50-1.70 (m, 2H), 1.82-1.90 (m, 2H), 2.73-2.88 (m, 2H), 3.90 (s, 3H), 3.94 (s, 6H), 4.15-4.30 (m, 2H), 4.43 (s, 2H), 6.33-6.39 (m, 1H), 6.52 (ddd, 1H, J=13.6 Hz, 6.4 Hz, 3.1 Hz), 6.98 (dd, 1H, J=19.1 Hz, 9.2 Hz), 7.11 (dd, 1H, J=5.0 Hz, 1.3 Hz), 7.16 (s, 2H), 7.51 (s, 1H), 8.58 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 174 Synthesis of 4-[N-(3,4-Difluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(3,4-difluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (534 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 442 mg (87%).

PREPARATION EXAMPLE 175 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(3,4-difluorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(3,4-difluorophenyl)amino]piperidine (625 mg) and 5-chloromethyl-3-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 350 mg (31%).

PREPARATION EXAMPLE 176 Synthesis of 4-[N-(3,4-Difluorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(3,4-difluorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine (350 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 305 mg (92%).

PREPARATION EXAMPLE 177 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(3,4-difluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(3,4-difluorophenyl)amino]piperidine (625 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (586 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 980 mg (86%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.52-1.66 (m, 2H), 1.81-1.89 (m, 2H), 2.72-2.85 (m, 2H), 3.78 (tt, 1H, J=11.8 Hz, 3.8 Hz), 3.88 (s, 3H), 3.90 (s, 6H), 4.12-4.30 (m, 2H), 4.45 (s, 2H), 6.36-6.42 (m, 1H), 6.54 (ddd, 1H, J=13.9 Hz, 6.8 Hz, 2.9 Hz), 6.71 (s, 2H), 6.95 (dd, 1H, J=19.2 Hz, 9.2 Hz), 7.20 (d, 1H, J=7.4 Hz), 7.36-7.43 (m, 3H).

PREPARATION EXAMPLE 178 Synthesis of 4-[N-(3,4-Difluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine Hydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(3,4-difluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine (980 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 819 mg (94%).

EXAMPLES 149 TO 156

 

These compounds were obtained by the condensation of amines obtained in Preparation Examples 174, 176 and 178 with chloride derivatives obtained in Preparation Examples 3, 42 and 48. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Exam- NMR data (400 MHz, measured as ple Structure Yield free bases, CDCl₃)δ 149

67% 1.70-1.90 (m, 4H), 2.16-2.23 (m, 2H), 2.95-3.03 (m, 2H), 3.58 (s, 2H), 3.64-3.74 (m, 1H), 3.89 (s, 3H), 3.90 (s, 3H), 3.93 (s, 6H), 3.96 (s, 6H), 4.49 (s, 2H), 6.31-6.37 (m, 1H), 6.51 (ddd, 1H, J=13.9Hz, 6.6Hz, 3.1Hz), 6.96 (dd, 1H, J=19.2Hz, 9.8Hz), #7.11 (d, 1H, J=5.1Hz), 7.15 (s, 2H), 7.20 (d, 1H, J=5.1Hz), 7.22 (s, 2H), 7.52 (s, 1H), 7.59 (s, 1H), 8.57 (d, 1H, J=5.1Hz), 8.59 (d, 1H, J=5.1Hz). 150

47% 1.67-1.79 (m, 2H), 1.81-1.89 (m, 2H), 2.13-2.20 (m, 2H), 2.95-3.05 (m, 2H), 3.59 (s, 2H), 3.63-3.75 (m, 1H), 3.89 (s, 3H), 3.90 (s, 3H), 3.93 (s, 12H), 4.47 (s, 2H), 6.30-6.36 (m, 1H), 6.50 (ddd, 1H, J=13.9Hz, 6.6Hz, 3.1Hz), 6.75 (s, 2H), 6.96 (d, 1H, J=19.0Hz, #9.4 Hz), 7.10 (d, 1H, J=4.1Hz), 7.15 (s, 2H), 7.51 (s, 1H), 7.75 (s, 1H), 8.50 (d, 1H, J=1.8Hz), 8.56 (d, 1H, J=5.1Hz), 8.70 (s, 1H). 151

53% 1.68-1.87 (m, 4H), 2.09-2.18 (m, 2H), 2.98-3.06 (m, 2H), 3.58 (s, 2H), 3.63-3.72 (m, 1H), 3.89 (s, 3H), 3.89 (s, 3H), 3.92 (s, 6H), 3.93 (s, 6H), 4.47 (s, 2H), 6.33-6.35 (m, 1H), 6.50 (ddd, 1H, J=13.9Hz, 6.4Hz, 2.9Hz), #6.76 (s, 2H), 6.95 (dd, 1H, J=19.2Hz, 9.4 Hz), 7.09 (d, 1H, J=5.1Hz), 7.15 (s, 2H), 7.25-7.30 (m, 1H), 7.37 (dd, 1H, J=7.3Hz, 7.3Hz), 7.42-7.46 (m, 2H), 7.50 (s, 1H), 8.56 (d, 1H, J=5.1Hz). 152

50% 1.72-1.96 (m, 4H), 2.12-2.28 (m, 2H), 2.94-3.08 (m, 2H), 3.59 (s, 2H), 3.62-3.72 (m, lH), 3.89 (s, 3H), 3.90 (s, 9H), 3.96 (s, 6H), 4.52 (s, 2H), 6.36-6.43 (m, 1H), 6.55 (ddd, 1H, J=13.7Hz, 6.6Hz, 2.9Hz), 6.67 (s, 2H), 6.96 (dd, 1H, J=19.1Hz, 9.2Hz), 7.21 (dd, #1H, J=5.1Hz, 1.2Hz), 7.24 (s, 2H), 7.61(br, 1H), 7.64 (s, 1H), 8.47 (d, 1H, J=2.0Hz), 8.60 (d, 1H, J=4.9 Hz), 8.67 (d, 1H, J=2.0Hz). 153

61% 1.7-1.90 (m, 4H), 2.12-2.25 (m, 2H), 2.95-3.05 (m, 2H), 3.57-3.75 (m, 1H), 3.59 (s, 2H), 3.88 (s, 3H), 3.90 (s, 9H), 3.93 (s, 6H), 4.50 (s, 2H), 6.32-6.43 (m, 1H), 6.54 (ddd, 1H, J=13.6Hz, 6.4Hz, 2.7Hz), 6.67 (s, 2H), 6.73-6.78 (m, 3H), 6.96 (dd, 1H, J=18.9Hz, #9.6Hz), 7.63 (s, 1H), 7.76 (s, 1H), 8.46 (s, 1H), 8.50 (d, 1H, J=1.6Hz), 8.66 (d, 1H, J=1.8Hz), 8.70 (d, 1H, J=2.0Hz). 154

82% 1.74-1.90 (m, 4H), 2.13-2.22 (m, 2H), 2.95-3.01 (m, 2H), 3.57 (s, 2H), 3.63-3.73 (m, 1H), 3.88 (s, 3H), 3.89 (s, 6H), 3.90 (s, 3H), 3.96 (s, 6H), 4.51 (s, 2H), 6.34-6.40 (m, 1H), 6.52 (ddd, 1H, J=14.1Hz, 6.6Hz, 3.1Hz), 6.70 (s, 2H), 6.94 (dd, 1H, J=19.2Hz, #9.4 Hz), 7.17-7.26 (m, 4H), 7.32-7.42 (m, 3H), 7.59 (s, 1H), 8.59 (d, 1H, J=5.1Hz). 155

75% 1.74-1.90 (m, 4H), 2.13-2.21 (m, 2H);2.95-3.04 (m, 2H), 3.59 (s, 2H), 3.63-3.72 (m, 1H), 3.88 (s, 3H), 3.89 (s, 6H), 3.89 (s, 3H), 3.93 (s, 6H), 4.49 (s, 2H), 6.33-6.39 (m, 1H), 6.52 (ddd, lH, J=14.3Hz, 3.7Hz, 2.9Hz), 6.69 (s, 2H), 6.75 (s, 2H), 6.94 (dd, #1H, J=19.1Hz, 9.8Hz), 7.19 (d, 1H, J=7.8Hz), 7.32-7.41 (m, 3H), 7.76 (s, 1H), 8.50 (d, 1H, J=1.5Hz), 8.69 (s, 1H). 156

79% 1.72-1.88 (m, 4H), 2.08-2.18 (m, 2H), 2.98-3.05 (m, 2H), 3.58 (s, 2H), 3.62-3.72 (m, 1H), 3.88 (s, 3H), 3.89 (s, 9H), 3.92 (s, 6H), 4.45 (s, 2H), 6.33-6.39 (m, 1H), 6.51 (ddd, 1H, J=13.9Hz, 6.6Hz, 3.0Hz), 6.69 (s, 2H), 6.76 (s, 2H), 6.93 (dd, 1H, J=19.3Hz, #9.5Hz), 7.19 (d, 1H, J=7.6Hz), 7.25-7.47 (m, 7H).

The chemical names of the compounds of Examples 149 to 156 are:

EXAMPLE 149

 

4-[N-(3,4-Difluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 150

 

4-[N-(3,4-Difluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 151

 

4-[N-(3,4-Difluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Dihydrochloride EXAMPLE 152

 

4-[N-(3,4-Difluorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 153

 

4-[N-(3,4-Difluorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 154

 

4-[N-(3,4-Difluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride EXAMPLE 155

 

4-[N-(3,4-Difluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Dihydrochloride EXAMPLE 156

 

4-[N-(3,4-Difluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Hydrochloride PREPARATION EXAMPLE 179 Synthesis of 1-(tert-Butoxycarbonyl)-4-[(4-fluorophenyl)amino]piperidine

1-(tert-Butoxycarbonyl)-4-piperidone (5.00 g) and 4-fluoroaniline (2.66 g) was treated in the same manner as described in Preparation Example 37 to give white crystalline powder of the title compound.

Yield: 4.99 g (71%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.23-1.36 (m, 2H), 1.46 (s, 9H), 1.97-2.05 (m, 2H), 2.84-2.96 (m, 2H), 3.30-3.39 (m, 2H), 3.96-4.14 (m, 2H), 6.51-6.57 (m, 2H), 6.84-6.91 (m, 2H).

PREPARATION EXAMPLE 180 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-fluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(4-fluorophenyl)amino]piperidine (589 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 702 mg (64%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.48-1.64 (m, 2H), 1.81-1.90 (m, 2H), 2.72-2.85 (m, 2H), 3.69-3.98 (m, 1H), 3.89 (m, 3H), 3.94 (m, 6H), 4.16-4.28 (m, 2H), 4.43 (s, 2H), 6.66-6.73 (m, 2H), 6.91 (dd, 2H, J=9.2 Hz, 9.2 Hz), 7.12-7.16 (m, 3H), 7.53 (s, 1H).

PREPARATION EXAMPLE 181 Synthesis of 4-[N-(4-Fluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-fluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (702 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 561 mg (84%).

PREPARATION EXAMPLE 182 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-fluorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(4-fluorophenyl)amino]piperidine (589 mg) and 5-chloromethyl-3-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 190 mg (17%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.50-1.73 (m, 2H), 1.82-1.90 (m, 2H), 2.71-2.85 (m, 2H), 3.71 (tt, 1H, J=11.7 Hz, 3.1 Hz), 3.89 (s, 3H), 3.90 (s, 6H), 4.12-4.30 (m, 2H), 4.45 (s, 2H), 6.66 (s, 2H), 6.73-6.78 (m, 2H), 6.91 (dd, 2H, J=9.2 Hz, 8.2 Hz), 7.65 (s, 1H), 8.49 (d, 1H, J=2.0 Hz), 8.65 (d, 1H, J=2.0 Hz).

PREPARATION EXAMPLE 183 Synthesis of 4-[N-(4-Fluorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-fluorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine (190 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 165 mg (91%).

PREPARATION EXAMPLE 184 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-fluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-[(4-fluorophenyl)amino]piperidine (589 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (586 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 1.01 g (92%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.44 (s, 9H), 1.51-1.65 (m, 2H), 1.82-1.90 (m, 2H), 2.82-2.84 (m, 2H), 3.78 (tt, 1H, J=11.7 Hz, 3.5 Hz), 3.88 (s, 3H), 3.90 (s, 6H), 4.10-4.30 (m, 2H), 4.45 (s, 2H), 6.68-6.73 (m, 4H), 6.89 (dd, 2H, J=9.2 Hz, 8.2 Hz), 7.21-7.25 (m, 1H), 7.32-7.41 (m, 3H).

PREPARATION EXAMPLE 185 Synthesis of 4-[N-(4-Fluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine Hydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-fluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine (1.01 g) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 790 mg (88%).

EXAMPLES 157 TO 164

 

These compounds were obtained by the condensation of amines obtained in Preparation Examples 181, 183 and 185 with chloride derivatives obtained in Preparation Examples 3, 42 and 48. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Exam- NMR data (400 MHz, measured as ple Structure Yield free bases, CDCl₃)δ 157

62% 1.60-1.82 (m, 2H), 1.83-1.91 (m, 2H), 2.13-2.23 (m, 2H), 2.95-3.03 (m, 2H), 3.57 (s, 2H), 3.64-3.75 (m, 1H), 3.89 (s, 3H), 3.90 (s, 3H), 3.93 (s, 6H), 3.96 (s, 6H), 4.48 (s, 2H), 6.65-6.70 (m, 2H), 6.90 (dd, 2H, J=8.8Hz, 8.8Hz), 7.13-7.16 (m, 3H), 7.20 (d, 1H, J=5.1Hz), 7.22 (s, 2H), 7.54 (s, 1H), 7.59 #(s, 1H), 8.55 (d, 1H, J=5.1Hz), 8.59 (d, 1H, J=4.9Hz). 158

53% 1.66-1.95 (m, 4H), 2.12-2.24 (m, 2H), 2.95-3.07 (m, 2H), 3.60 (s, 2H), 3.64-3.76 (m, 1H), 3.89 (s, 3H), 3.90 (s, 3H), 3.92 (s, 6H), 3.93 (s, 6H), 4.47 (s, 2H), 6.63-6.70 (m, 1H), 6.75 (s, 2H), 6.90 (dd, 1H, J=9.2Hz), 7.11-7.16 (m, 3H), 7.53 (s, 1H), 7.77 (s,1H), 8.50 (d, 1H, J=2.0 Hz), 8.55 (d, 1H, J=4.9Hz), #8.70 Hz), (d, 1H, J=5.9Hz). 159

51% 1.64-1.90 (m, 4H), 2.07- 2.20 (m, 4H), 2.97-3.08 (m, 2H), 3.59 (s, 2H), 3.64-3.76 (m, 1H), 3.89 (s, 6H), 3.92 (s, 6H), 3.93 (s, 6H), 4.47 (s, 2H), 6.62- 6.70 (m, 2H), 6.77 (s, 2H), 6.86-6.93 (m, 2H), 7. 1 1 - 7.16 (m, 3H), 7.25-7.31 (m, 3H), 7.37 (dd, 1H, J=7.4Hz, 7.4Hz), #7.42- 7.49 (m, 2H), 7.53 (s, 1H), 8.54 (d, 1H, J=5.1Hz). 160

49% 1.74-1.98 (m, 4H), 2.10- 2.30 (m, 2H), 2.90-3.12 6H), 3.90 (s, 3H), 3.96 (s, 6H), 4.50 (s, 2H), 6.66 (s, 2H), 6.70-6.76 (m, 2H), 6.90 (dd, 2H, J=8.8Hz, 8.8Hz), 7.19-7.28 (m, 3H), 7.65 (br, 2H), 8.49 (d, 1H, J=1.8Hz), 8.60 (d, 1H, J=4.9Hz), 8.64 (d, 1H, J=2.2Hz). 161

26% 1.67-1.97 (m, 4H), 2.10- 2.27 (m, 2H), 2.94-3.06 (m, 2H), 3.56-3.68 (m, 3H), 3.88 (s, 3H), 3.89 (s, 6H), 3.90 (s, 3H), 3.93 (s, 6H), 4.49 (s, 2H), 6.65 (s, 2H), 6.69-6.80 (m, 4H), 6.84-6.93 (m, 2H), 7.64 (s, 1H), 7.77 (br, 1H), 8.48 (d, 1H, J=1.7Hz), #8.50 (d, 1H, J=1.7Hz), 8.64 (d, 1H, J=1.9Hz), 8.70 (s, 1H). 162

83% 1.72-1.92 (m, 4H), 2.12- 2.21 (m, 2H), 2.94-3.02 (m, 2H), 3.57 (s, 2H), 3.64-3.74 (m, 1H), 3.88 (s, 3H), 3.89 (s, 6H), 3.90 (s, 3H), 3.96 (s, 6H), 4.51 (s, 1H), 6.66-6.71 (m, 4H), 6.88 (dd, 2H, J=8.6Hz, 8.6Hz), 7.18-7.27 (m, 4H), 7.34 (dd, 1H, #J=7.4 Hz, 7.4Hz), 7.39 (d, 2H, J=5.4Hz), 7.59 (s, 1H), 8.59 (d, 1H, J=5.1Hz). 163

68% 1.68-1.87 (m, 4H), 2.10-2.22 (m, 2H), 2.94-3.04 (m, 2H), 3.59 (s, 2H), 3.65-3.74 (m, 1H), 3.87 (s, 3H), 3.88 (s, 6H), 3.90 (s, 3H), 3.93 (s, 6H), 4.49 (s, 2H), 6.66-6.70 (m, 6H), 6.88 (dd, 2H, J=8.8Hz, 8.8Hz), 7.19-7.40 (m, 4H), 7.77 (s, 1H), 8.49 (d, 1H, j=1.8Hz), 8.70 (s, 1H). 164

74% 1.70-1.90 (m, 4H), 2.08-2.18 (m, 2H), 2.95-3.05 (m, 2H), 3.58 (s, 2H), 3.63-3.73 (m, 1H), 3.87 (s, 3H), 3.88 (s, 6H), 3.89 (s, 3H), 3.92 (s, 6H), 4.50 (s, 2H), 6.65-6.72 (m, 2H), 6.69 (s, 2H), 6.76 (s, 2H), 6.87 (dd, 2H, J=9.0 Hz, 9.0Hz), 7.22 (d, 1H, J=7.6 Hz), 7.25-7.48 (m, 9H).

The chemical names of the compounds of Examples 157 to 164 are:

EXAMPLE 157

 

4-[N-(4-Fluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 158

 

4-[N-(4-Fluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 159

 

4-[N-(4-Fluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Dihydrochloride EXAMPLE 160

 

4-[N-(4-Fluorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 161

 

4-[N-(4-Fluorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 162

 

4-[N-(4-Fluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride EXAMPLE 163

 

4-[N-(4-Fluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Dihydrochloride EXAMPLE 164

 

4-[N-(4-Fluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine Hydrochloride PREPARATION EXAMPLE 186 Synthesis of 1-(tert-Butoxycarbonyl)-4-phenylaminopiperidine

1-(tert-Butoxycarbonyl)-4-piperidone (5.00 g) and aniline (2.23 g) was treated in the same manner as described in Preparation Example 37 to give white needles of the title compound.

Yield: 3.77 g (57%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.25-1.38 (m, 2H), 1.47 (s, 9H), 2.00-2.07 (m, 2H), 2.87-2.97 (m, 2H), 3.38-3.53 (m, 2H), 3.96-4.14 (m, 2H), 6.57-6.52 (m, 2H), 6.70 (tt, 1H, J=6.2 Hz, 1.0 Hz), 7.17 (dd, 2H, J=8.6 Hz, 7.2 Hz).

PREPARATION EXAMPLE 187 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-phenyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-phenylaminopiperidine (553 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 760 mg (71%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.53-1.63 (m, 2H), 1.83-1.91 (m, 2H), 2.76-2.90 (m, 2H), 3.86-3.97 (m, 1H), 3.89 (s, 3H), 3.93 (s, 6H), 4.14-4.32 (m, 2H), 4.49 (s, 2H), 6.71-6.78 (m, 3H), 7.14 (s, 1H), 7.15 (s, 2H), 7.21 (dd, 2H, J=8.8 Hz, 7.4 Hz), 7.55 (s, 1H), 8.56 (d, 1H, J=5.1 Hz).

PREPARATION EXAMPLE 188 Synthesis of 4-[N-Phenyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-phenyl-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (760 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 652 mg (90%).

PREPARATION EXAMPLE 189 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-phenyl-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-phenylaminopiperidine (553 mg) and 5-chloromethyl-3-(3,4,5-trimethoxyphenyl)pyridine (588 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 222 mg (21%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.52-1.67 (m, 2H), 1.82-1.91 (m, 2H), 2.74-2.87 (m, 2H), 3.88-3.90 (m, 1H), 3.88 (s, 3H), 3.89 (s, 6H), 4.144.31 (m, 2H), 4.53 (s, 2H), 6.67 (s, 2H), 6.74-6.80 (m, 3H), 7.21 (dd, 2H, J=8.8 Hz, 7.2 Hz), 7.67 (s, 1H), 8.50 (d, 1H, J=5.3 Hz, 2.2 Hz), 8.66 (d, 1H, J=2.1 Hz).

PREPARATION EXAMPLE 190 Synthesis of 4-[N-Phenyl-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-phenyl-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]piperidine (222 mg) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 197 mg (94%).

PREPARATION EXAMPLE 191 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-phenyl-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine

1-(tert-Butoxycarbonyl)-4-phenylaminopiperidine (553 mg) and 3-(3,4,5-trimethoxyphenyl)benzyl chloride (586 mg) was treated in the same manner as described in Example 9 to give light yellow amorphous of the title compound.

Yield: 1.06 g (100%). ¹H-NMR (400 MHz, CDCl₃) δ: 1.45 (s, 9H), 1.52-1.68 (m, 2H), 1.83-1.92 (m, 2H), 2.73-2.86 (m, 2H), 3.88 (s, 3H), 3.89 (s, 6H), 3.94 (tt, 1H, J=11.7 Hz, 3.3 Hz), 4.14-4.30 (m, 2H), 4.52 (s, 2H), 6.69-6.78 (m, 6H), 7.17-7.27 (m, 2H), 7.32-7.42 (m, 3H).

PREPARATION EXAMPLE 192 Synthesis of 4-[N-Phenyl-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine Hydrochloride

1-(tert-Butoxycarbonyl)-4-[N-phenyl-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]piperidine (1.06 g) was treated in the same manner as described in Preparation Example 94 to give light yellow powder of the title compound.

Yield: 909 mg (97%).

EXAMPLES 165 TO 169

 

These compounds were obtained by the condensation of amines obtained in Preparation Examples 188, 190 and 192 with chloride derivatives obtained in Preparation Examples 3 and 48. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Exam- NMR data (400 MHz, measured as ple Structure Yield free bases, CDCl₃)δ 165

53% 1.63-1.81 (m, 4H), 1.82-1.92 (m, 2H), 2.14-2.24 (m, 2H), 2.95-3.05 (m, 2H), 3.59 (s, 2H), 3.80-4.02 (m, 1H), 3.89 (s, 3H), 3.90 (s, 3H), 3.92 (s, 6H), 3.93 (s, 6H), 4.53 (s, 2H), 6.69-6.77 (m, 5H), 7.13-7.17 (m, 3H), 7.20 (dd, 2H, J=7.6Hz, 7.6Hz), 7.55 (s, 1H), 7.76 (s, #1H), 8.51 (d, 1H, J=1.8Hz), 8.55 (d, 1H, J=5.1Hz), 8.70 (s, 1H). 166

50% 1.85-2.04 (m, 4H), 2.20-2.40 (m, 2H), 2.92-3.25 (m, 2H), 3.60-3.77 (m, 3H), 3.88 (s, 3H), 3.89 (s, 6H), 3.90 (s, 3H), 3.97 (s, 6H), 4.59 (s, 2H), 6.67 (s, 2H), 6.72-6.81 (m, 4H), 7.17-7.30 (m, 4H), 7.68 (s, 1H), 8.50 (s, 1H), 8.62 (d, 1H, J=4.9Hz), 8.65 (d, 1H, J=2.0Hz). 167

43% 1.72-1.92 (m, 4H), 2.13-2.26 (m, 2H), 2.95-3.04 (m, 2H), 3.59 (s, 2H), 3.78-4.01 (m, 1H), 3.88 (s, 9H), 3.90 (s, 3H), 3.93 (s, 6H), 4.56 (s, 2H), 6.66 (s, 2H), 6.70-6.78 (m, 5H), 7.19 (dd, 2H, J=8.2Hz, 8.2Hz), 7.66 (s, 1H), 7.77 (s, 1H), 8.50 (d, 1H, J=2.3 Hz), 8.51 (d, 1H, J=2.2Hz), #8.65 (d, 1H, J=1.9Hz), 8.70 (d, 1H, J=2.2Hz). 168

82% 1.75-1.92 (m, 4H), 2.14-2.23 (m, 2H), 2.94-3.01 (m, 2H), 3.57 (s, 2H), 3.80-3.94 (m, 1H), 3.87 (s, 3H), 3.88 (s, 6H), 3.90 (s, 3H), 3.96 (s, 6H), 4.57 (s, 2H), 6.67-6.77 (m, 5H), 7.15-7.27 (m, 5H), 7.34 (dd, 1H, J=7.4Hz, 7.4 Hz), 7.39 (d, 1H, 7.6Hz), 7.42 (s, 1H), 7.59 (s, 1H), 8.59 (d, #1H, J=5.1Hz). 169

65% 1.72-1.91 (m, 4H), 2.13-2.22 (m, 2H), 2.95-3.03 (m, 2H), 3.59 (s, 2H), 3.79-4.00 (m, 1H), 3.87 (s, 3H), 3.87 (s, 6H), 3.90 (s, 3H), 3.93 (s, 6H), 4.56 (s, 2H), 6.66-6.77 (m, 7H), 7.18 (dd, 2H, J=7.4Hz, 7.4Hz), 7.24 (d, 1H, J=7.4Hz), 7.33 (dd, 1H, J=7.4Hz, 7.4Hz), 7.38 (d, 1H, #J=7.6Hz), 7.41 (s, 1H), 7.76 (s, 1H), 8.50 (d, 1H, J=1.6Hz), 8.69 (d, 1H, J=2.2 Hz).

The chemical names of the compounds of Examples 165 to 169 are:

EXAMPLE 165

 

4-[N-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-N-phenylamino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 166

 

4-[N-[[3-(3,4,5-Trimethoxyphenyl)pyridin-5-yl]methyl]-N-phenylamino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 167

 

4-[N-[[3-(3,4,5-Trimethoxyphenyl)pyridin-5-yl]methyl]-N-phenylamino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Trihydrochloride EXAMPLE 168

 

4-[N-[3-(3,4,5-Trimethoxyphenyl)benzyl]-N-phenylamino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Dihydrochloride EXAMPLE 169

 

4-[N-[3-(3,4,5-Trimethoxyphenyl)benzyl]-N-phenylamino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine Dihydrochloride

Preparation Example Structure NMR data (400 MHz, CDCl₃)δ 193

4.61 (s, 2H), 7.25 (d, 1H, J=1.2Hz), 7.41-7.52 (m, 3H), 7.75 (d, 1H, J=0.8Hz), 7.98-8.02 (m, 2H), 8.69 (d, 1H, J=4.9Hz). 194

3.87 (s, 3H), 4.60 (s, 2H), 7.01 (d, 1H, J=8.4 Hz), 7.08 (t, 1H, J=7.4Hz), 7.24 (dd, 1H, J=5.1Hz, 1.4Hz), 7.38 (dt, 1H, J=7.4Hz, 1.8Hz), 7.77 (dd, 1H, J=7.6Hz, 1.8Hz), 7.84 (s, 1H), 8.69 (d, 1H, J=5.1Hz) 195

3.90 (s, 3H), 4.60 (s, 2H), 6.87-7.03 (1H, m), 7.39 (t, 1H, 7.8Hz), 7.50-7.66 (m, 2H), 7.73 (s, 1H), 8.68 (d, 1H, J=5.1Hz) 196

1.45 (t, 3H, J=7.0Hz), 4.12 (q, 2H, J=7.0Hz), 4.59 (s, 2H), 6.99 (d, 2H, J=8.8Hz), 7.18 (d, 1H, J=5.1Hz), 7.20-7.29 (m, 1H), 7.68 (s, 1H), 7.95 (d, 2H, J=8.8Hz), 8.63 (d, 1H, J=5.1Hz) 197

3.95 (s, 3H), 4.00 (s, 3H), 4.60 (s, 2H), 6.96 (d, 1H, J=8.4Hz), 7.21 (d, 1H, J=4.1Hz), 7.53 (dd, 1H, J=8.4Hz, 2.0Hz), 7.67 (d, 1H, J=2.0Hz), 7.70 (s, 1H), 8.65 (d, 1H, J=5.1Hz) 198

4.61 (s, 2H), 7.14-7.21 (m, 1H.), 7.21-7.23 (m, 2H), 7.35-7.42 (m, 1H), 7.80 (s, 1H), 7.98 (1H, dt, J=8.0Hz, 2.0Hz), 8.73 (d, 1H, J=5.1Hz) 199

4.61 (s, 2H), 7.13 (1H, dt, J=8.4Hz, 2.8Hz), 7.28 (1H, d, J=5.0Hz), 7.40-7.79 (m, 1H), 7.70-7.79 (m, 3H), 8.69 (d, 1H, J=5.0Hz) 200

4.60 (s, 2H), 7.13-7.20 (m, 2H), 7.25 (1H, d, J=5.1Hz), 7.70 (s, 1H), 7.95-8.03 (m, 2H), 8.66 (d, 1H, J=5.1Hz) 201

4.61 (s, 2H), 7.21-7.30 (m, 2H), 7.69 (s, 1H), 7.73-7.76 (m, 1H), 7.85-7.92 (m, 1H), 8.76 (d, 1H, J=4.9Hz) 202

4.61 (s, 2H), 6.86-6.91 (m, 1H), 7.31 (1H, d, J=5.1Hz), 7.51-7.59 (m, 2H), 7.71 (s, 1H), 8.69 (d, 1H, J=5.1Hz) 203

4.61 (s, 2H), 7.26 (d, 1H, J=4.9Hz), 7.45 (d, 2H, J=8.4Hz), 7.72 (s, 1H), 7.95 (d, 2H, J=8.4Hz), 8.68 (s, 1H, J=4.9Hz)

PREPARATION EXAMPLE 204 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[(2-phenylpyridin-4-yl)methyl]amino]piperidine

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (612 mg) and 4-chloromethyl-2-phenylpyridine (204 mg) were condensed in the same manner as described in Example 9 to give the title compound.

Yield: 407 mg (43%).

PREPARATION EXAMPLE 205 Synthesis of 4-[N-(4-Methoxyphenyl)-N-[(2-phenylpyridin-4-yl)methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[(2-phenylpyridin-4-yl)methyl]amino]piperidine (407 mg) was treated in the same manner as described in Preparation Example 94 to give the title compound.

Yield: 365 mg (95%).

PREPARATION EXAMPLE 206 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[[2-(2-methoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (306 mg) and 4-chloromethyl-2-(2-methoxyphenyl)pyridine (234 mg) were condensed in the same manner as described in Example 9 to give the title compound.

Yield: 237mg (72%).

PREPARATION EXAMPLE 207 Synthesis of 4-[N-(4-Methoxyphenyl)-N-[[2-(2-methoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[[2-(2-methoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (360 mg) was treated in the same manner as described in Preparation Example 94 to give the title compound.

Yield: 365mg (65%).

PREPARATION EXAMPLE 208 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[[2-(3-methoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (306 mg) and 4-chloromethyl-2-(3-methoxyphenyl)pyridine (234 mg) were condensed in the same manner as described in Example 9 to give the title compound.

Yield: 550mg (theoretical yield).

PREPARATION EXAMPLE 209 Synthesis of 4-[N-(4-Methoxyphenyl)-N-[[2-(3-methoxyphenyl)pyridin-4-yl]methyl]amino]piperidin e Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[[2-(3-methoxyphenyl)pyridin-4-yl]methyl]amino]piperidine (550 mg) was treated in the same manner as described in Preparation Example 94 to give the title compound.

Yield: 436g (85%).

PREPARATION EXAMPLE 210 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[2-(4-ethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (306 mg) and 4-chloromethyl-2-(4-ethoxyphenyl)pyridine (248 mg) were condensed in the same manner as described in Example 9 to give the title compound.

Yield: 515 mg (99%).

PREPARATION EXAMPLE 211 Synthesis of 4-[N-[[2-(4-Ethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-[2-(4-ethoxyphenyl)pyridin-4-yl]methyl-N-(4-methoxyphenyl)amino]piperidine (515 mg) was treated in the same manner as described in Preparation Example 94 to give the title compound.

Yield: 418 mg (80%).

PREPARATION EXAMPLE 212 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-(4-methoxyphenyl)-N-[[2-(3,4-dimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (306 mg) and 4-chloromethyl-2-(3,4-dimethoxyphenyl)pyridine (264 mg) were condensed in the same manner as described in Example 9 to give the title compound.

Yield: 600 mg (theoretical yield).

PREPARATION EXAMPLE 213 Synthesis of 4-[N-[[2-(3,4-Dimethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-[[2-(3,4-dimethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine (600 mg) was treated in the same manner as described in Preparation Example 94 to give the title compound.

Yield: 416 mg (77%).

PREPARATION EXAMPLE 214 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[[2-(2-fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (306 mg) and 4-chloromethyl-2-(2-fluorophenyl)pyridine (222 mg) were condensed in the same manner as described in Example 9 to give the title compound.

Yield: 530 mg (theoretical yield).

PREPARATION EXAMPLE 215 Synthesis of 4-[N-[[2-(2-Fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-[[2-(2-fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine (530 mg) was treated in the same manner as described in Preparation Example 94 to give the title compound.

Yield: 423mg (85%).

PREPARATION EXAMPLE 216 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[[2-(3-fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (153 mg) and 4-chloromethyl-2-(3-fluorophenyl)pyridine (111 mg) were condensed in the same manner as described in Example 9 to give the title compound.

Yield: 270 mg (theoretical yield).

PREPARATION EXAMPLE 217 Synthesis of 4-[N-[[2-(3-Fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine Dihydrochloride;

1-(tert-Butoxycarbonyl)-4-[N-[[2-(3-fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine (270 mg) was treated in the same manner as described in Preparation Example 94 to give the title compound.

Yield: 193 mg (70%).

PREPARATION EXAMPLE 218 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[[2-(4-fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (306 mg) and 4-chloromethyl-2-(4-fluorophenyl)pyridine (222 mg) were condensed in the same manner as described in Example 9 to give the title compound.

Yield: 550 mg (theoretical yield).

PREPARATION EXAMPLE 219 Synthesis of 4-[N-[[2-(4-Fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[N-[[2-(4-fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine (550 mg) was treated in the same manner as described in Preparation Example 94 to give the title compound.

Yield: 439 mg (88%).

PREPARATION EXAMPLE 220 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[[2-(3,4-difluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (306 mg) and 4-chloromethyl-2-(3,4-difluorophenyl)pyridine (240 mg) were condensed in the same manner as described in Example 9 to give the title compound.

Yield: 590 mg (theoretical yield).

PREPARATION EXAMPLE 221 Synthesis of 4-[N-[[2-(3,4-Difluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine Dihydrochloride

1-(tert-Butoxycarbonyl)-4-[-N-[[2-(3,4-difluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine (590 mg) was treated in the same manner as described in Preparation Example 94 to give the title compound.

Yield: 483 mg (93%).

PREPARATION EXAMPLE 222 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[[2-(3,5-difluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (306 mg) and 4-chloromethyl-2-(3,5-difluorophenyl)pyridine (240 mg) were condensed in the same manner as described in Example 9 to give the title compound.

Yield: 530 mg (theoretical yield).

PREPARATION EXAMPLE 223 Synthesis of 4-[N-[[2-(3,5-Difluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine Dihydrochloride;

1-(tert-Butoxycarbonyl)-4-[N-[[2-(3,5-difluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine: (530 mg) was treated in the same manner as described in Preparation Example 94 to give the title compound.

Yield: 418 mg (81%).

PREPARATION EXAMPLE 224 Synthesis of 1-(tert-Butoxycarbonyl)-4-[N-[[2-(4-chlorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine;

4-(p-Anisidino)-1-(tert-butoxycarbonyl)piperidine (306 mg) and 4-chloromethyl-2-(4-chlorophenyl)pyridine (238 mg) were condensed in the same manner as described in Example 9 to give the title compound.

Yield: 600 mg (theoretical yield).

PREPARATION EXAMPLE 225 Synthesis of 4-[N-[[2-(4-Chlorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine Dihydrochloride;

1-(tert-Butoxycarbonyl)-4-[N-[[2-(4-chlorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine: (600 mg) was treated in the same manner as described in Preparation Example 94 to give the title compound.

Yield: 447 mg (86%).

EXAMPLES 170 TO 202

 

These compounds were obtained by the condensation of amines obtained in Preparation Examples 96, 205, 207, 209, 211, 213, 215, 217, 219, 221, 223 and 225 with chloride derivatives obtained in Preparation Examples 3, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102 and 103. Free bases obtained were then converted to the corresponding hydrochlorides. Yields and NMR data of their free bases are listed below.

Ex- am- NMR data (400 MHz, measured as ple Structure Yield free bases, CDCl₃) δ 170

 47% 1.67-1.80(m, 2H), 1.83-1.91(m, 2H), 2.10-2.19(m, 2H), 2.93-3.00 (m, 2H), 3.54-3.65(m, 1H), 3.56 (s, 2H), 3.73(s, 3H), 3.89(s, 3H), 3.93(s, 6H), 4.45(s, 3H), 6.73(d, 2H, J=9.4Hz), 6.78(d, 2H, J=9.4 Hz), 7.14-7.21(m, 2H), 7.15(s, 2H), 7.38-7.49(m, 3H), 7.57(s, 1H), 7.68(s, 1H), 7.97(d, 1H, J=1.0Hz), 7.99(d, 1H, J=1.6Hz), 8.54(d, 1H, J=5.1Hz), 8.61(d, 1H, J=5.1Hz). 171

 55% 1.62-1.80(m, 2H), 1.84-1.93(m, 2H), 2.10-2.20(m, 2H), 2.93-3.02 (m, 2H), 3.53-3.66(m, 1H), 3.56 (s, 2H), 3.73(s, 3H), 3.90(s, 3H), 3.96(s, 6H), 4.44(s, 2H), 6.65-6.83(m, 4H), 7.14-7.30(m, 4H), 7.36-7.50(m, 3H), 7.59(s, 1H), 7.67(s, 1H), 7.93(d, 2H, J=7.0Hz), 8.54-8.61(m, 2H). 172

 54% 1.67-1.92(m, 4H), 2.08-2.20(m, 2H), 2.92-3.01(m, 2H), 3.52-3.65 (m, 1H), 3.55(s, 2H), 3.72(s, 3H), 4.38(s, 2H), 6.72(d, 2H, J=9.2 Hz), 6.78(d, 2H, J=9.0Hz), 7.18 (dd, 2H, J=4.9Hz, 4.9Hz), 7.36-7.50(m, 6H), 7.67(s, 1H), 7.68(s, 1H), 7.93(dd, 2H, J=8.4 Hz, 1.2Hz), 7.98(dd, 2H, J=8.6 Hz, 1.4Hz), 8.57(d, 1H, J=5.1 Hz), 8.60(d, 1H, J=5.1Hz). 173

100% 1.66-1.79(m, 2H), 1.82-1.91(m, 2H), 2.09-2.20(m, 2H), 2.93-3.03 (m, 2H), 3.56(s, 2H), 3.56-3.59 (m, 1H), 3.73(s, 3H), 3.80(s, 3H), 3.89(s, 3H), 3.93(s, 6H), 4.45(s, 2H), 6.73(d, 2H, J=9.3Hz), 6.78 (d, 2H, J=9.3Hz), 6.98(d, 1H, J=8.5Hz), 7.07(t, 1H J=7.6Hz), 7.15(s, 2H), 7.15-7.19(m, 2H), 7.33-7.38(m, 1H), 7.57(s, 1H), 7.66-7.74(m, 2H), 8.53(d, 1H, J=5.1Hz), 8.61(d, 1H, J=4.9Hz). 174

 94% 1.70-1.80(m, 2H), 1.83-1.91(m, 2H), 2.11-2.18(m, 2H), 2.92-3.01 (m, 2H), 3.56(s, 2H), 3.57-3.65 (m, 1H), 3.73(s, 3H), 3.74(s, 3H), 3.90(s, 3H), 3.96(s, 6H), 4.44(s, 2H), 6.71(d, 2H, J=9.0Hz), 6.78 (d, 2H, J=9.0Hz), 6.96(d, 1H, J=8.3Hz), 7.05(dt, 1H. J=7.3Hz, 1.0Hz), 7.14(d, 1H, J=5.2Hz), 7.20(d, 1H, J=5.2Hz), 7.22(2H, s), 7.32-7.37(m, 1H), 7.59(s, 1H), 7.71-7.75(m, 2H), 8.56-8.60(m, 2H). 175

 98% 1.67-1.80(m, 2H), 1.83-1.90(m, 2H), 2.10-2.19(m, 2H), 2.94-3.03 (m, 2H), 3.50-3.67(m, 1H), 3.56 (s, 2H), 3.73(s, 3H), 3.74(s, 3H), 3.79(s, 3H), 4.44(s, 2H), 6.70(d, 2H, J=9.3Hz), 6.78(d, 2H, J=9.3 Hz), 6.96(d, 1H, J=8.3Hz), 6.98 (d, 1H, J=8.8Hz), 7.04(dd, 1H, J=7.6Hz, 1.0Hz), 7.07(dd, 1H, 7.6, J=1.0Hz), 7.12-7.19(m, 2H), 7.32-7.39(m, 2H), 7.70-7.75(m, 4H), 8.58(d, 1H, J=5.1Hz), 8.61 (d, 1H, J=4.9H #). 176

100% 1.68-1.79(m, 2H), 1.82-1.90(m, 2H), 2.10-2.19(m, 2H), 2.90-3.01 (m, 2H), 3.56(s, 2H), 3.56-3.58 (m, 1H), 3.73(s, 3H), 3.89(s, 3H), 3.91(s, 3H), 3.93(s, 6H), 4.45(s, 2H), 6.73(d, 2H, J=9.3Hz), 6.78 (d, 2H, J=9.3Hz), 6.93-6.99(m, 1H), 7.15(s, 2H), 7.16-7.20(m, 2H), 7.37(t, 1H, J=7.8Hz), 7.52-7.59(m, 3H), 7.67(s, 1H), 8.54(d, 1H, J=5.1Hz), 8.60(d, 1H, J=5.1Hz). 177

100% 1.68-1.79(m, 2H), 1.83-1.92(m, 2H), 2.11-2.16(m, 2H), 2.91-3.02 (m, 2H), 3.56(s, 2H), 3.55-3.65 (m, 1H), 3.73(s, 3H), 3.88(s, 3H), 3.90(s, 3H), 3.96(s, 6H), 4.43(s, 2H), 6.72(d, 2H, J=9.3Hz), 6.78 (d, 2H, J=9.3Hz), 6.95(dd, 1H. J=8.3Hz, 2.7Hz), 7.16-7.21(m, 2H), 7.22(s, 2H), 7.35(t, 1H, J=7.8Hz), 7.48(d, 1H, J=7.8Hz), 7.53(t, 1H, J=2.7Hz), 7.59(s, 1H), 7.65(s, 1H), 8.55-8.60(m, 2H). 178

100% 1.65-1.79(m, 2H), 1.82-1.90(m, 2H), 2.09-2.19(m, 2H), 2.92-3.00 (m, 2H), 3.50-3.66(m, 1H), 3.56 (s, 2H), 3.73(s, 3H), 3.73(s, 3H), 3.88(s, 3H), 3.89(s, 3H), 4.44(s, 2H), 6.72(d, 2H, J=9.3Hz), 6.78 (d, 2H, J=9.3Hz), 6.92-6.98(m, 2H), 7.16-7.21(m, 2H), 7.34(d, 1H, J=7.8Hz), 7.38(d, 1H, J=8.5 Hz), 7.46-7.59(m, 4H), 7.65(s, 1H), 7.67(s, 1H), 8.57(dd, 1H, J=5.1Hz, 0.7Hz), 8.60(d, 1H, J=5.1Hz). 179

 76% 1.44(t, 3H, J=7.1Hz), 1.70-1.80 (m, 2H), 1.82-1.91(m, 2H), 2.10-2.19(m, 2H), 2.90-3.02(m, 2H), 3.54(s, 2H), 3.73-3.78(m, 1H), 3.73(s, 3H), 3.88(s, 3H), 3.93(s, 6H), 4.09(q, 2H, J=7.1 Hz), 4.45(s, 2H), 6.73(d, 2H, J=9.2Hz), 6.78(d, 2H, J=9.2Hz), 6.97(d, 2H, J=8.8Hz), 7.10-7.18 (m, 2H), 7.15(s, 2H), 7.57(s, 1H), 7.61(s, 1H), 7.92(d, 2H, J=8.8 Hz), 8.52-8.58(m, 2H). 180

 93% 1.43(t, 3H, J=6.8Hz), 1.68-1.80 (m, 2H), 1.82-1.92(m, 2H), 2.10-2.19(m, 2H), 2.90-3.01(m, 2H), 3.56(s, 2H), 3.57-3.64(m, 1H), 3.73(s, 3H), 3.90(s, 3H), 3.96(s, 6H), 4.08(q, 2H, J=6.8 Hz), 4.42(s, 2H), 6.72(d, 2H, J=9.0Hz), 6.78(d, 2H, J=9.3Hz), 6.95(d, 2H, J=8.8Hz), 7.11(d, 1H, J=5.1Hz), 7.20(d, 1H, J=5.1 Hz), 7.22(s, 2H), 7.58-7.62(m, 2H), 7.87(d, 2H, J=8.8Hz), 8.52 d, 1H, J=5.1Hz), 8.58(d, 1H, #J=5.1Hz). 181

100% 1.43(t, 3H, J=7.1Hz), 1.44(t, 3H, J=7.1Hz), 1.67-1.78(m, 2H), 1.82-1.90(m, 2H), 2.09-2.18(m, 2H), 2.92-3.00(m, 2H), 3.54(s, 2H), 3.55-3.65(m, 1H), 3.73(s, 3H), 4.08(q, 2H, J=7.1Hz), 4.09 (q, 2H, J=6.8Hz), 4.42(s, 2H), 6.71(d, 2H, J=9.0Hz), 6.78(d, 2H, J=9.0Hz), 6.93-7.00(m, 4H), 7.10-7.14(m, 2H), 7.60(s, 2H), 7.88(s, 2H), 7.88(d, 2H, J=8.8 Hz), 7.93(d, 2H, J=8.8Hz), 8.52 5.1Hz), 8.56(d, 1H, J=4.9Hz) #. 182

100% 1.68-1.79(m, 2H), 1.82-1.90(m, 2H), 2.10-2.19(m, 2H), 2.90-3.01 (m, 2H), 3.55(s, 2H), 3.56-3.59 (m, 1H), 3.73(s, 3H), 3.89(s, 3H), 3.93(s, 6H), 3.94(s, 3H), 3.99(s, 3H), 4.45(s, 2H), 6.76(d, 2H, J=9.5Hz), 6.78(d, 2H, J=9.5Hz), 6.94(d, 1H, J=8.3Hz), 7.15(s, 2H), 7.16-7.19(m, 2H), 7.49-7.66 (m, 4H), 8.54(d, 1H, J=4.9Hz), 8.57(d, 1H, J=5.1Hz). 183

100% 1.68-1.78(m, 2H), 1.82-1.91(m, 2H), 2.10-2.18(m, 2H), 2.93-3.00 (m, 2H), 3.56(s, 2H), 3.56-3.62 (m, 1H), 3.73(s, 3H), 3.90(s, 3H), 3.93(s, 3H), 3.96(s, 6H), 3.97(S, 3H), 4.43(s, 2H), 6.72(d, 2H, J=9.3Hz), 6.78(d, 2H, J=9.3Hz), 6.92(d, 1H, J=8.3Hz), 7.12(d, 1H, J=5.1Hz), 7.20(d, 1H, J=5.1 Hz), 7.22(s, 2H), 7.42(d, 1H, J=8.5Hz, 2.2Hz), 7.58-7.63(m, 3H), 8.53(d, 1H, J=4.9Hz), 8.58 (d, 1H, J=5.1Hz). 184

 89% 1.67-1.79(m, 2H), 1.84-1.90(m, 2H), 2.10-2.19(m, 2H), 2.93-3.01 (m, 2H), 3.50-3.65(m, 1H), 3.55 (s, 2H), 3.73(s, 3H), 3.94(s, 3H), 3.97(s, 3H), 3.99(s, 3H), 4.43(s, 2H), 6.72(d, 2H, J=9.3Hz), 6.78 (d, 2H, J=9.3Hz), 6.92(d, 1H, J=8.6Hz), 6.94(d, 1H, J=8.3Hz), 7.14(d, 1H, J=5.6Hz), 7.15(d, 1H, J=6.4Hz), 7.43(dd, 1H, J=8.6 Hz, 2.0Hz), 7.50(dd, 1H, J=8.3 Hz, 1.9Hz), 7.60-7.63(m, 3H), 7.66(d, 1H, J=2.2Hz #), 8.53(d, 1H, J=5.1Hz), 8.57(d, 1H, J=4.9 Hz). 185

100% 1.68-1.79(m, 2H), 1.82-1.90(m, 2H), 2.10-2.20(m, 2H), 2.93-3.01 (m, 2H), 3.57(s, 2H), 3.57-3.65 (m, 1H), 3.73(s, 3H), 3.89(s, 3H), 3.93(s, 6H), 4.46(s, 2H), 6.73(d, 2H, J=7.3Hz), 6.78(d, 2H, J=7.3 Hz), 7.11-7.19(m, 2H), 7.15(s, 2H), 7.22-7.29(m, 2H), 7.34-7.40 (m, 1H), 7.58(s, 1H), 7.73(s, 1H), 7.94(t, 1H, J=8.3Hz), 8.54(d, 1H, J=5.1Hz), 8.64(d, 1H, J=4.9 Hz). 186

 88% 1.68-1.79(m, 2H), 1.83-1.92(m, 2H), 2.09-2.16(m, 2H), 2.93-3.01 (m, 2H), 3.56(s, 2H), 3.56-3.62 (m, 1H), 3.73(s, 3H), 3.90(s, 3H), 3.96(s, 6H), 4.44(s, 2H), 6.71(d, 2H, J=9.3Hz), 6.77(d, 2H, J=9.3 Hz), 7.10-7.16(m, 1H), 7.17-7.26 (m, 3H), 7.22(s, 2H), 7.32-7.38 (m, 1H), 7.59(s, 1H), 7.73(s, 1H), 7.92(dt, 1H, J=8.0Hz, 2.0 Hz), 8.57-8.61(m, 2H). 187

100% 1.66-1.80(m, 2H), 1.83-1.93(m, 2H), 2.10-2.20(m, 2H), 2.92-3.02 (m, 2H), 3.53-3.65(m, 1H), 3.57 (s, 2H), 3.73(s, 3H), 4.44(s, 2H), 6.71(d, 2H, J=9.0Hz), 6.78(d, 2H, J=9.3Hz), 7.10-7.18(m, 2H), 7.19-7.29(m, 4H), 7.32-7.40(m, 2H), 7.73(s, 2H), 7.91(dd, 1H, J=8.1Hz, 1.4Hz), 7.95(dd, 1H, J=7.6Hz, 1.5Hz), 8.60(d, 1H, J=4.9Hz), 8.64(d, 1H, J=5.1Hz). 188

 96% 1.67-1.80(m, 2H), 1.82-1.92(m, 2H), 2.10-2.20(m, 2H), 2.91-3.01 (m, 2H), 3.56(s, 2H), 3.56-3.61(m, 1H), 3.73(s, 3H), 3.89(s, 3H), 3.93(s, 6H), 4.46(s, 2H), 6.73(d, 2H, J=9.3Hz), 6.78 (d, 2H, J=9.3Hz), 7.06-7.19(m, 2H), 7.15(s, 2H), 7.20-7.26(m, 1H), 7.38-7.45(m, 1H), 7.56 (s, 1H), 766-7.78(m, 3H), 8.54(d, 1H, J=5.1Hz), 8.61(d, 1H, J=4.9 Hz). 189

 92% 1.65-1.78(m, 2H), 1.79-1.92(m, 2H), 2.21-2.26(m, 2H), 2.90-3.01 (m, 2H), 3.56(s, 2H), 3.56-3.63 (m, 1H), 3.73(s, 3H), 3.90(s, 3H), 3.96(s, 6H), 4.44(s, 2H), 6.72(d, 2H, J=9.3Hz), 6.78(d, 2H, J=9.3 Hz), 7.08(dt, 1H, J=8.3Hz, 1.7 Hz), 7.18-7.40(m, 2H), 7.22(s, 2H), 7.37-7.43(m, 1H), 7.56-7.72 (m, 4H), 8.55-8.60(m, 2H). 190

 55% 1.66-1.79(m, 2H), 1.80-1.91(m, 2H), 2.10-2.20(m, 2H), 2.88-3.01 (m, 2H), 3.50-3.66(m, 1H), 3.56 (s, 2H), 3.73(s, 3H), 4.45(s, 2H), 6.72(d, 2H, J=8.5Hz), 6.79(d, 2H, J=9.0Hz), 7.04-7.13(m, 2H), 7.19-7.25(m, 2H), 7.35-7.46(m, 2H), 7.62-7.79(m, 6H), 8.57(d, 1H, J=5.1Hz), 8.61(d, 1H, J=4.9 Hz). 191

100% 1.68-1.79(m, 2H), 1.82-1.91(m, 2H), 2.10-2.19(m, 2H), 2.92-3.00 (m, 2H), 3.55(s, 2H), 3.56-3.63 (m, 1H), 3.73(s, 3H), 3.89(s, 3H), 3.93(s, 6H), 4.45(s, 2H), 6.73(d, 2H, J=9.3Hz), 6.78(d, 2H, J=9.3 Hz), 7.11-7.19(m, 4H), 7.15(s, 2H), 7.57(s, 1H), 7.63(s, 1H), 7.92-8.01(m, 2H), 8.54(d, 1H, J=5.1Hz), 8.58(d, 1H, J=5.1Hz). 192

100% 1.68-1.79(m, 2H), 1.83-1.92(m, 2H), 2.11-2.19(m, 2H), 2.93-3.01 (m, 2H), 3.56(s, 2H), 3.57-3.62 (m, 1H), 3.73(s, 3H), 3.90(s, 3H), 3.96(s, 6H), 4.43(s, 2H), 6.72(d, 2H, J=9.3Hz), 6.78(d, 2H, J=9.3 Hz), 7.10-7.22(m, 4H), 7.22(s, 2H), 7.54-7.66(m, 2H), 7.88-7.94 (m, 2H), 8.55(d, 1H, J=4.9Hz), 8.58(d, 1H, J=4.9Hz). 193

 90% 1.66-1.80(m, 2H), 1.83-1.91(m, 2H), 2.10-2.19(m, 2H), 2.92-3.00 (m, 2H), 3.50-3.66(m, 1H), 3.55 (s, 2H), 3.73(s, 3H), 4.44(s, 2H), 6.72(d, 2H, J=9.3Hz), 7.78(d, 2H, J=9.3Hz), 7.09-7.20(m, 6H), 7.62(s, 1H), 7.63(s, 1H), 7.89-8.00(m, 4H), 8.55(d, 1H, J=5.1Hz), 8.58(d, 1H, J=4.9Hz). 194

 36% 1.68-1.80(m, 2H), 1.82-1.90(m, 2H), 2.11-2.19(m, 2H), 2.91-2.99 (m, 2H), 3.55(s, 2H), 3.56-3.62 (m, 1H), 3.73(s, 3H), 3.89(s, 3H), 3.93(s, 6H), 4.45(s, 2H), 6.73(d, 2H, J=9.3Hz), 6.78(d, 2H, J=9.3 Hz), 7.15(s, 2H), 7.16-7.26(m, 3H), 7.57(s, 1H), 7.62(s, 1H), 7.71(br, 1H), 7.80-7.90(m, 1H), 8.54(d, 1H, J=5.1Hz), 8.58(d, 1H, J=4.9Hz). 195

100% 1.60-1.80(m, 2H), 1.82-1.91(m, 2H), 2.12-2.19(m, 2H), 2.91-3.00 (m, 2H), 3.56(s, 2H), 3.56-3.64 (m, 1H), 3.73(s, 3H), 3.90(s, 3H), 3.96(s, 6H), 4.45(s, 2H), 6.72(d, 2H, J=9.0Hz), 6.78(d, 2H, J=9.0 Hz), 7.17-7.24(m, 4H), 7.25-7.27 (m, 1H), 7.60(s, 2H), 7.65(br, 1H), 7.77-7.84(m, 1H), 8.53-8.61 (m, 2H). 196

100% 1.66-1.79(m, 2H), 1.82-1.91(m, 2H), 2.09-2.20(m, 2H), 2.90-3.00 (m, 2H), 3.50-3.65(m, 1H), 3.55 (s, 2H), 3.73(s, 3H), 4.44(s, 2H), 6.72(d, 2H, J=9.3Hz), 6.79(d, 2H, J=9.3Hz), 7.18-7.28(m, 4H), 7.60(s, 1H), 7.62(s, 1H), 7.63-7.68(m, 1H), 7.70-7.75(m, 1H), 7.77-7.89(m, 2H), 8.55(d, 1H, J=4.9Hz), 8.58(d, 1H, J=5.1 Hz.) 197

100% 1.68-1.80(m, 2H), 1.82-1.90(m, 2H), 2.10-2.21(m, 2H), 2.90-3.00 (m, 2H), 3.56(s, 2H), 3.56-3.63 (m, 1H), 3.73(s, 3H), 3.89(s, 3H), 3.93(s, 6H), 4.56(s, 2H), 6.73(d, 2H, J=9.3Hz), 6.78(d, 2H, J=9.3 Hz), 6.81-6.87(m, 1H), 7.15(s, 2H), 7.18(d, 1H, J=4.2Hz), 7.22-7.26(m, 1H), 7.51-7.59(m, 3H), 7.65(s, 1H), 8.54(d, 1H, J=4.9Hz), 8.59(d, 1H, J=5.1Hz). 198

100% 1.65-1.79(m, 2H), 1.80-1.94(m, 2H), 2.22-2.25(m, 2H), 2.90-3.05 (m, 2H), 3.56(s, 2H), 3.56-3.65 (m, 1H), 3.73(s, 3H), 3.90(s, 3H), 3.96(s, 6H), 4.44(s, 2H), 6.72(d, 2H, J=9.2Hz), 6.78(d, 2H, J=9.2 Hz), 6.80-6.94(m, 2H), 7.22(s, 2H), 7.19-7.28(m, 1H), 7.45-7.51 (m, 2H), 7.59(s, 1H), 7.62(s, 1H), 8.56(d, 1H, J=4.9Hz), 8.59(d, 1H, J=5.1Hz). 199

100% 1.67-1.79(m, 2H), 1.82-1.92(m, 2H), 2.12-2.20(m, 2H), 2.92-2.99 (m, 2H), 3.50-3.65(m, 1H), 3.56 (s, 2H), 3.73(s, 3H), 4.45(s, 2H), 6.72(d, 2H, J=9.0Hz), 6.79(d, 2H, J=9.3Hz), 6.80-6.88(m, 2H), 7.23-7.27(m, 2H), 7.48(dd, 2H, J=8.8Hz, 2.2Hz), 7.55(dd, 2H, J=8.8Hz, 2.2Hz), 7.63(s, 1H), 7.65(s, 1H), 8.57(d, 1H, J=4.9 Hz), 8.60(d, 1H, J=4.9Hz). 200

 84% 1.68-1.80(m, 2H), 1.83-1.92(m, 2H), 2.10-2.21(m, 2H), 2.91-3.00 (m, 2H), 3.56(s, 2H), 3.57-3.62 (m, 1H), 3.73(s, 3H), 3.89(s, 3H), 3.93(s, 6H), 4.45(s, 2H), 6.73(d, 2H, J=9.3Hz), 6.78(d, 2H, J=9.3 Hz), 7.15(s, 2H), 7.17(d, 1H, J=4.9Hz), 7.20(d, 1H, J=5.1Hz), 7.43(d, 2H, J=8.3Hz), 7.57(s, 1H), 7.65(s, 1H), 7.93(d, 2H, J=8.3Hz), 8.54(d, 1H, J=4.9Hz), 8.59(d, 1H, J=5.1Hz). 201

 72% 1.65-1.78(m, 2H), 1.82-1.91(m, 2H), 2.10-2.16(m, 2H), 2.91-3.02 (m, 2H), 3.56(s, 2H), 3.56-3.64 (m, 1H), 3.73(s, 3H), 3.90(s, 3H), 3.96(s, 6H), 4.43(s, 2H), 6.72(d, 2H, J=9.3Hz), 6.78(d, 2H, J=9.3 Hz), 7.17-7.21(m, 1H), 7.22(2H, s), 7.41(d, 2H, J=8.7Hz), 7.48(d, 1H, J=7.8Hz), 7.59(s, 1H), 7.63 (s, 1H) 7.87(d, 2H, J=8.7Hz), 8.5(d, 1H, J=4.9Hz), 8.58(d, 1H, J=5.1Hz). 202

 94% 1.67-1.88(m, 2H), 1.83-1.90(m, 2H), 2.10-2.17(m, 2H), 2.92-2.99 (m, 2H), 3.50-3.65(m, 1H), 3.55 (s, 2H), 3.73(s, 3H), 4.44(s, 2H), 6.72(d, 2H, J=9.0Hz), 6.78(d, 2H, J=9.3Hz), 7.17-7.22(m, 2H), 7.39-7.45(m, 4H), 7.63(s, 1H), 7.65(s, 1H), 7.88(d, 2H, J=8.6 Hz), 7.93(d, 2H, J=8.5Hz), 8.56 (d, 1H, J=4.9Hz), 8.59(d, 1H, J=4.9Hz).

The chemical names of the compounds of Examples 170 to 202 are:

EXAMPLE 170

 

4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin4-yl]methyl]amino]-1-[(2-phenylpyridin-4-yl)methyl]piperidine Trihydrochloride EXAMPLE 171

 

4-[N-(4-Methoxyphenyl)-N-[(2-phenylpyridin-4-yl)methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 172

 

4-[N-(4-Methoxyphenyl)-N-[(2-phenylpyridin-4-yl)methyl]amino]-1-[(2-phenylpyridin-4-yl)methyl]piperidine Trihydrochloride EXAMPLE 173

 

4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(2-methoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 174

 

4-[N-(4-Methoxyphenyl)-N-[[2-(2-methoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 175

 

4-[N-(4-Methoxyphenyl)-N-[[2-(2-methoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(2-methoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 176

 

4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3-methoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 177

 

4-[N-(4-Methoxyphenyl)-N-[[2-(3-methoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 178

 

4-[N-(4-Methoxyphenyl)-N-[[2-(3-methoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3-methoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 179

 

1-[[2-(4-Ethoxyphenyl)pyridin-4-yl]methyl]-4-[N-(4-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Trihydrochloride EXAMPLE 180

 

4-[N-[[2-(4-Ethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 181

 

1-[[2-(4-Ethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[[2-(4-ethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine Trihydrochloride EXAMPLE 182

 

4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4-dimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 183

 

4-[N-(4-Methoxyphenyl)-N-[[2-(3,4-dimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 184

 

4-[N-(4-Methoxyphenyl)-N-[[2-(3,4-dimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4-dimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 185

 

1-[[2-(2-Fluorophenyl)pyridin-4-yl]methyl]-4-[N-(4-methoxyphenyl)-N-[[2-(3,4,5-trimethoxy phenyl)pyridin-4-yl]methyl]amino]piperidine Trihydrochloride EXAMPLE 186

 

4-[N-[[2-(2-Fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 187

 

4-[N-[[2-(2-Fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(2-fluorophenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 188

 

1-[[2-(3-Fluorophenyl)pyridin-4-yl]methyl]-4-[N-(4-methoxyphenyl)-N-[[2,4,5-trimethoxy phenyl)pyridin-4-yl]methyl]amino]piperidine Trihydrochloride EXAMPLE 189

 

4-[N-[[2-(3-Fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 190

 

4-[N-[[2-(3-Fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3-fluorophenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 191

 

1-[[2-(4-Fluorophenyl)pyridin-4-yl]methyl]-4-[N-(4-methoxyphenyl)-N-[[2-(3,4,5-trimethoxy phenyl)pyridin-4-yl]methyl]amino]piperidine Trihydrochloride EXAMPLE 192

 

4-[N-[[2-(4-Fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 193

 

4-[N-[[2-(4-Fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(4-fluorophenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 194

 

1-[[2-(3,4-Difluorophenyl)pyridin-4-yl]methyl]-4-[N-(4-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Trihydrochloride EXAMPLE 195

 

4-[N-[[2-(3,4-Difluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 196

 

4-[N-[[2-(3,4-Difluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,4-difluorophenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 197

 

1-[[2-(3,5-Difluorophenyl)pyridin-4-yl]methyl]-4-[N-(4-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Trihydrochloride EXAMPLE 198

 

4-[N-[[2-(3,5-Difluorophenyl)pyridin-4-yl]methyl-N-(4-methoxyphenyl)amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 199

 

4-[N-[[2-(3,5-Difluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,5-difluorophenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 200

 

1-[[2-(4-Chlorophenyl)pyridin-4-yl]methyl]-4-[N-(4-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine Trihydrochloride EXAMPLE 201

 

4-[N-[[2-(4-Chlorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride EXAMPLE 202

 

4-[N-[[2-(4-Chlorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(4-chlorophenyl)pyridin-4-yl]methyl]piperidine Trihydrochloride TEST EXAMPLE 1 Inhibitory Effect on Cell Adhesion

The test was conducted by reference to the method by Ross et al. (J. Biol. Chem., 267 8537-8543 (1992)). More specifically, after human umbilical venous endothelial cells (HUVEC) were cultured on a 48-well plate to confluent growth, TNFα was added thereto. Upon elapsed time of 5 hours after the addition, U937, which was a human monocytic/histocytic cell fluorescence-labeled with PKH2 (product of Sigma-Aldrich Co., Ltd.), was added in a proportion of 1×10⁶ cells per well. After the plate was left at rest at room temperature for 1 hour, unadhered U937 was washed out and lysed in 1% Triton X-100 to measure a remaining fluorescence intensity (excitation wavelength: 480 nm; measuring wavelength: 530 nm). HUVEC and U937 were cultured in EGM-2 (product of Sanko Junyaku K. K.) and 10% FCS-containing RPMI1640, respectively. Each test agent was added to HUVEC upon the addition of TNFα and to U937 24 hours prior to the cell adhesion test. The inhibitory activity was calculated out as IC₅₀ value after inhibitory ratio at each concentration of test compounds was determined. The inhibitory ratio was calculated according to the equation [(C−B)/(A−B)×100 (%)], wherein A is the number of U937 cells adhered to HUVEC stimulated by TNFα when no test agent was added, B is the number of U937 cells adhered to HUVEC not stimulated by TNFα when no test agent was added, and C is the number of U937 cells adhered to HUVEC stimulated by TNFα when the test agent was added. The results are shown in Table 1. As control compounds, Test Compound 1 described in Japanese Patent Application Laid-Open No. 9-143075 and dilazep described in Japanese Patent Application Laid-Open No. 11-92382 were simultaneously evaluated.

TABLE 1 Example IC₅₀ (μM) 3 0.3 5 0.2 7 0.3 10 0.04 13 0.03 16 0.3 19 0.3 23 0.03 29 0.03 36 0.2 40 0.2 42 0.07 67 0.09 88 0.07 89 0.09 111 0.08 157 0.09 Test compound 1 10 Dilazep >10

As mentioned above, the compound of the present invention is characterized in that the cyclic amine has two phenyl-pyridyl or biphenyl groups, or phenyl-pyridyl and biphenyl groups. The inhibitory effect on cell adhesion of the cyclic amine compound having pyridyl groups at the both ends thereof obtained in Preparation Example 91 was examined similar to the above procedure. As the result, the compound was inactive even at a concentration as high as 10 μM.

Specific formulation examples will hereinafter be described.

EXAMPLE 203

 

Capsule Preparation

Compound obtained by Example 13  30 mg Microcrystalline cellulose  30 mg Lactose  57 mg Magnesium stearate  3 mg Total amount  120 mg.

The above ingredients were mixed in accordance with a method known per se in the art and then charged in capsules to obtain capsule preparations.

EXAMPLE 204

 

Tablet Preparation

Compound obtained by Example 13  30 mg Starch  44 mg Starch (for glue) 5.6 mg Magnesium stearate 0.4 mg Calcium carboxymethyl cellulose  20 mg Total amount 100 mg.

The above ingredients were mixed in accordance with a method known per se in the art to obtain tablet preparations.

EXAMPLE 205

 

Injection Preparation

Compound obtained by Example 13(100 mg) and sodium chloride (900 mg) were dissolved in distilled water (about 80 mL) for injection, and distilled water for injection was added to the resultant solution to 100 mL in total. This diluted solution was sterilized by filtration and then subdivided and charged into 10 ampoules, and the ampoules were sealed to obtain injection preparations.

As described above, the compounds (1) according to the present invention have inhibitory effects on both cell adhesion and cell infiltration and are useful as medicines for prevention or treatment of allergy, asthma, rheumatism, arteriosclerosis, inflammatory, Sjogren's syndrome, etc.

Obviously, numerous modifications of the above teachings are apparent to those skilled in the art. Therefore, within the scope of the appended claims the invention may be practiced otherwise than as specifically described herein. 

What is claimed is:
 1. A cyclic amine selected from the group consisting of: 4-[N-(4-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzoyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine, 4-[N-(4-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzoyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine, 4-[N-(4-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzoyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine, 4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine dihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine dihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine hydrochloride, 4-[N-(4-Ethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Ethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Ethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine dihydrochloride, 4-[N-(4-Ethoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Ethoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Ethoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine dihydrochloride, 4-[N-(4-Ethoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine dihydrochloride, 4-[N-(4-Ethoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine hydrochloride, 4-[N-(4-Butoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Butoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Butoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine dihydrochloride, 4-[N-(4-Butoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Butoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Butoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine dihydrochloride, 4-[N-(4-Butoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine dihydrochloride, 4-[N-(4-Butoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine hydrochloride, 4-[N-(3-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(3-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(3-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine dihydrochloride, 4-[N-(3-Methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(3-Methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(3-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine dihydrochloride, 4-[N-(3-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine dihydrochloride, 4-[N-(3-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine hydrochloride, 4-[N-(2-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(2-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(2-Methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(2-Methoxyphenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(2-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine dihydrochloride, 4-[N-(2-Methoxyphenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine dihydrochloride, 4-[N-(2,3-Dimethoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-[4-(Trifluoromethoxy)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-[4-(Trifluoromethoxy)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-[4-(Trifluoromethoxy)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine dihydrochloride, 4-[N-[4-(Trifluoromethoxy)phenyl]-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-[4-(Trifluoromethoxy)phenyl]-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-[4-(Trifluoromethoxy)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine dihydrochloride, 4-[N-[4-(Trifluoromethoxy)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine dihydrochloride, 4-[N-[4-(Trifluoromethoxy)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine hydrochloride, 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methylthiophenyl)amino]piperidine trihydrochloride, 1-[[3-(3,4,5-Trimethoxyphenyl)pyridin-5-yl]methyl]-4-[N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methylthiophenyl)amino]piperidine trihydrochloride, 1-[3-(3,4,5-Trimethoxyphenyl)benzyl]-4-[N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methylthiophenyl)amino]piperidine dihydrochloride, 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]-N-(4-methylthiophenyl)amino]piperidine trihydrochloride, 1-[[3-(3,4,5-Trimethoxyphenyl)pyridin-5-yl]methyl]-4-[N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]-N-(4-methylthiophenyl)amino]piperidine trihydrochloride, 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[3-(3,4,5-trimethoxyphenyl)benzyl]-N-(4-methylthiophenyl)amino]piperidine dihydrochloride, 1-[[3-(3,4,5-Trimethoxyphenyl)pyridin-5-yl]methyl]-4-[N-[3-(3,4,5-trimethoxyphenyl)benzyl ]-N-(4-methylthiophenyl)amino]piperidine dihydrochloride, 1-[3-(3,4,5-Trimethoxyphenyl)benzyl]-4-[N-[3-(3,4,5-trimethoxyphenyl)benzyl]-N-(4-methylthiophenyl)amino]piperidine hydrochloride, 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methylphenyl)amino]piperidine trihydrochloride, 1-[[3-(3,4,5-Trimethoxyphenyl)pyridin-5-yl]methyl]-4-[N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methylphenyl)amino]piperidine trihydrochloride, 1-[3-(3,4,5-trimethoxyphenyl)benzyl]-4-[N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methylphenyl)amino]piperidine dihydrochloride, 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]-N-(4-methylphenyl)amino]piperidine trihydrochloride, 1-[[3-(3,4,5-Trimethoxyphenyl)pyridin-5-yl]methyl]-4-[N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]-N-(4-methylphenyl)amino]piperidine trihydrochloride, 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[3-(3,4,5-trimethoxyphenyl)benzyl]-N-(4-methylphenyl)amino]piperidine dihydrochloride, 1-[[3-(3,4,5-Trimethoxyphenyl)pyridin-5-yl]methyl]-4-[N-[3-(3,4,5-trimethoxyphenyl)benzyl]-N-(4-methylphenyl)amino]piperidine dihydrochloride, 1-[3-(3,4,5-Trimethoxyphenyl)benzyl]-4-[N-[3-(3,4,5-trimethoxyphenyl)benzyl]-N-(4-methylphenyl)amino]piperidine hydrochloride, 4-[N-[4-(Trifluoromethyl)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-[4-(Trifluoromethyl)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-[4-(Trifluoromethyl)phenyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine dihydrochloride, 4-[N-[4-(Trifluoromethyl)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine dihydrochloride, 4-[N-(4-(Trifluoromethyl)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine dihydrochloride, 4-[N-[4-(Trifluoromethyl)phenyl]-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine hydrochloride, 4-[N-(4-Bromophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Bromophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Bromophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine dihydrochloride, 4-[N-(4-Bromophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Bromophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Bromophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine dihydrochloride, 4-[N-(4-Bromophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine dihydrochloride, 4-[N-(4-Bromophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine hydrochloride, 4-[N-(4-Chlorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Chlorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Chlorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine dihydrochloride, 4-[N-(4-Chlorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Chlorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Chlorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine dihydrochloride, 4-[N-(4-Chlorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine dihydrochloride, 4-[N-(4-Chlorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine hydrochloride, 4-[N-(3,4-Difluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(3,4-Difluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(3,4-Difluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine dihydrochloride, 4-[N-(3,4-Difluorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(3,4-Difluorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(3,4-Difluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine dihydrochloride, 4-[N-(3,4-Difluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine dihydrochloride, 4-[N-(3,4-Difluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine hydrochloride, 4-[N-(4-Fluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Fluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Fluorophenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine dihydrochloride, 4-[N-(4-Fluorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Fluorophenyl)-N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]amino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Fluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine dihydrochloride, 4[N-(4Fluorophenyl)-N-[3(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[3-(3,4,5trimethoxyphenyl)pyridin-5-yl]methyl]piperidine dihydrochloride, 4-[N-(4-Fluorophenyl)-N-[3-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[3-(3,4,5-trimethoxyphenyl)benzyl]piperidine hydrochloride, 4-[N[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-N-phenylamino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]-N-phenylamino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]-N-phenylamino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine trihydrochloride, 4-[N-[3-(3,4,5-trimethoxyphenyl)benzyl]-N-phenylamino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine dihydrochloride, 4-[N-[3-(3,4,5-trimethoxyphenyl)benzyl]-N-phenylamino]-1-[[3-(3,4,5-trimethoxyphenyl)pyridin-5-yl]methyl]piperidine dihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[(2-phenylpyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[(2-phenylpyridin-4-yl)methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[(2-phenylpyridin-4-yl)methyl]amino]-1-[(2-phenylpyridin-4-yl) methyl]piperidine trihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(2-methoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[[2-(2-methoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[[2-(2-methoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(2-methoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3-methoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[[2-(3-methoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[[2-(3-methoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3-methoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 1-[[2-(4-Ethoxyphenyl)pyridin-4-yl]methyl]-4-[N-(4-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine trihydrochloride, 4-[N-[[2-(4-Ethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 1-[[2-(4-Ethoxyphenyl)pyridin-4-yl]methyl]-4-[N-[[2-(4-ethoxyphenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]piperidine trihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4-dimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[[2-(3,4-dimethoxyphenyl)pyridin-4-yl]methyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-(4-Methoxyphenyl)-N-[[2-(3,4-dimethoxyphenyl)pyridin-4-yl]methyl]amino]-[[2-(3,4-dimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 1-[[2-(2-Fluorophenyl)pyridin-4-yl]methyl]-4-[N-(4-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine trihydrochloride, 4-[N-[[2-(2-Fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-[[2-(2-Fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(2-fluorophenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 1-[[2-(3-Fluorophenyl)pyridin-4-yl]methyl]-4-[N-(4-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine trihydrochloride, 4-[N-[[2-(3-Fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-[[2-(3-Fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3-fluorophenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 1-[[2-(4-Fluorophenyl)pyridin-4-yl]methyl]-4-[N-(4-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine trihydrochloride, 4-[N-[[2-(4-Fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-[[2-(4-Fluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(4-fluorophenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 1-[[2-(3,4-Difluorophenyl)pyridin-4-yl]methyl]-4-[N-(4-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine trihydrochloride, 4-[N-[[2-(3,4-Difluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-[[2-(3,4-Difluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,4-difluorophenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 1-[[2-(3,5-Difluorophenyl)pyridin-4-yl]methyl]-4-[N-(4-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine trihydrochloride, 4-[N-[[2-(3,5-Difluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-[[2-(3,5-Difluorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,5-difluorophenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 1-[[2-(4-Chlorophenyl)pyridin-4-yl]methyl]-4-[N-(4-methoxyphenyl)-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amino]piperidine trihydrochloride, 4-[N-[[2-(4-Chlorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, 4-[N-[[2-(4-Chlorophenyl)pyridin-4-yl]methyl]-N-(4-methoxyphenyl)amino]-1-[[2-(4-chlorophenyl)pyridin-4-yl]methyl]piperidine trihydrochloride, and salts thereof and hydrates thereof.
 2. A pharmaceutical composition which comprises as an active ingredient a cyclic amine compound selected from the group consisting of the compounds of claim 1, salts thereof and hydrates thereof, and a pharmaceutically acceptable carrier.
 3. A method for treating a disease caused by cell adhesion and/or cell infiltration, which comprises administering an effective amount of a cyclic amine compound selected from the group consisting of the compounds of claim 1, salts thereof and hydrates thereof.
 4. The pharmaceutical composition according to claim 2, comprising said active ingredient in an amount effective for treating a disease caused by cell adhesion and/or cell infiltration.
 5. The pharmaceutical composition according to claim 4, wherein said disease is selected from allergy, asthma, inflammation, rheumatic disease, arteriosclerosis and Sjogren's syndrome.
 6. The method according to claim 3, wherein said disease is selected from allergy, asthma, inflammation, rheumatic disease, arteriosclerosis and Sjogren's syndrome. 